Month: March 2021

Each compound has different characteristics, and only by selecting the characteristics of the compound suitable for a specific situation can the compound be applied on a large scale. 27492-84-8, name is Methyl 4-amino-2-methoxybenzoate, This compound has unique chemical properties. The synthetic route is as follows., HPLC of Formula: C9H11NO3

A solution of 1-({5-chloro-2-[(2-methylpropyl)oxy]phenyl}methyl)-5-methyl-1 H-pyrazole-3- carboxylic acid (807 mg), methyl 4-amino-2-methoxybenzoate (453 mg), N-(3- dimethylaminopropyl)-N’-ethylcarbodiimide hydrochloride (516 mg) and 1- hydroxybenzotriazole hydrate (406 mg) in dichloromethane (10 ml) and dimethylformamide (10 ml) was stirred at ambient temperature for 24 hours. Ethyl acetate (60 ml) was added and the mixture washed with water (60 ml), saturated sodium bicarbonate solution (25 ml) and brine (2 x 20 ml), dried (MgSO4) and concentrated in vacuo. The residue was purified by SP4 Biotage chromatography using 5 to 40percent ethyl acetate in hexane to afford the title compound (738 mg, 61percent) as a white foamy solid. LC/MS [MH+] = 486/488, RT = 3.70 min.

Chemical properties determine the actual use. Each compound has specific chemical properties and uses. We look forward to more synthetic routes in the future to expand reaction routes of 27492-84-8.

Reference:
Patent; GLAXO GROUP LIMITED; WO2006/114313; (2006); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Researchers who often do experiments know that organic synthesis is a process of preparing more complex target molecules from simple raw materials through one or more chemical reactions. Generally, it requires fewer steps, and cheap raw materials. 2475-81-2, name is Methyl 2-amino-4-fluorobenzoate, A new synthetic method of this compound is introduced below., Safety of Methyl 2-amino-4-fluorobenzoate

Example 14A methyl 2-(benzylamino)-4-fluorobenzoate Methyl 2-amino-4-fluorobenzoate (0.90 g), benzaldehyde (0.54 mL), sodium triacetoxyborohydride (1.58 g) and acetic acid (0.3 mL) in CH2Cl2 (20 mL) were stirred for 3 hours. The reaction was quenched with methanol, concentrated, and chromatographed on silica gel with 5% ethyl acetate/hexanes.

The basis of chemical reaction formula synthesis, the synthesis route is composed of some specific reactions and combined according to certain logical thinking. We look forward to the emergence of more reaction modes in the future.

Reference:
Patent; ABBOTT LABORATORIES; US2010/184750; (2010); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

These common heterocyclic compound, 335599-07-0, name is Ethyl 3-oxa-bicyclo[3.1.0]hexane-6-carboxylate, its traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc, below Introduce a new synthetic route. name: Ethyl 3-oxa-bicyclo[3.1.0]hexane-6-carboxylate

Production Example 11-2(3-Oxa-bicyclo[3.1.0]hex-6-yl)methanol diastereomer 1 3-Oxa-bicyclo[3.1.0]hexane-6-carboxylic acid ethyl ester diastereomer 1 (10 g, 64.1 mmol) was dissolved in TIM (100 mL), and to the mixture, was added dropwise a 0.99M toluene (180 mL, 178 mmol) solution of DIBAL while cooling on ice, and stirred at room temperature for one hour. To the reaction mixture, were added a small amount of water and ethyl acetate, and the mixture was filtered with Celite, washed with ethyl acetate, and then the filtrate was distilled off under reduced pressure, and the residue was purified by column chromatography (heptane:ethyl acetate to 75% ethyl acetate) to obtain the title compound (2.6 g, 228 mmol) as a colorless oil.1H-NMR (CDCl3) delta: 1.10 (dt, J=3.6 Hz, 6.8 Hz, 1H), 1.53-1.56 (m, 2H), 3.53 (d, J=6.8 Hz, 2H), 3.70 (d, J=8.0 Hz, 2H), 3.88 (d, J=8.4 Hz, 2H)Production Example 11-3(3-Oxa-bicyclo[3.1.0]hex-6-yl)methanol diastereomer 2 From 3-oxa-bicyclo[3.1.0]hexane-6-carboxylic acid ethyl ester diastereomer 2 (5 g, 32.1 mmol), the title compound (2.1 g, 18.4 mmol) was obtained as a colorless oil according to the same procedure as in (3-oxa-bicyclo[3.1.0]hex-6-yl)methanol diastereomer 1.1H-NMR (CDCl3) delta: 1.23 (t, J=3.6 Hz, 1H), 1.80 (d, J=3.6 Hz, 2H), 3.79 (d, J=7.6 Hz, 2H), 3.91 (m, 4H)

The synthetic route of Ethyl 3-oxa-bicyclo[3.1.0]hexane-6-carboxylate has been constantly updated, and we look forward to future research findings.

Reference:
Patent; Eisai R&D Management Co., Ltd.; US2011/86882; (2011); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Each compound has different characteristics, and only by selecting the characteristics of the compound suitable for a specific situation can the compound be applied on a large scale. 1195768-18-3, name is Methyl 3-amino-2-fluorobenzoate, This compound has unique chemical properties. The synthetic route is as follows., category: esters-buliding-blocks

General procedure: To a solution of PTMA (1d) (29.0 mg, 0.10 mmol) and aminobenzoates 2 (1.5 mmol or 0.20 mmol) in DMF (1.0 mL) at room temperature were added Et3N or pyridine (0.42 mmol) and HATU(76.1 mg, 0.20 mmol). The mixture was stirred at room temperature overnight and monitored by TLC. Then brine (10 mL) was added.The resulting mixture was extracted with EtOAc (3 5.0 mL), andthe combined organic portions were dried over anhydrous sodium sulfate and concentrated in vacuo. compounds 3 were finally prepared through flash column chromatography (eluent: EtOAc/lightpetroleum ether 1:20e5:1).

According to the analysis of related databases, 1195768-18-3, the application of this compound in the production field has become more and more popular.

Reference:
Article; Qiu, Lin; Tian, Kai; Pan, Jian; Jiang, Lin; Yang, Hu; Zhu, Xiangcheng; Shen, Ben; Duan, Yanwen; Huang, Yong; Tetrahedron; vol. 73; 6; (2017); p. 771 – 775;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Application of 33689-29-1,Some common heterocyclic compound, 33689-29-1, name is Methyl 1-hydroxycyclopropanecarboxylate, molecular formula is C5H8O3, traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc, below Introduce a new synthetic route.

Copper (I) iodide (650 mg, 3.41 mmol) and triethylamine (3.0 mL, 22 mmol) were added to a stirred solution of methyl 1-hydroxycyclopropanecarboxylate (2.0 g, 17.22 mmol) in acetonitrile (60 mL) at rt in a sealed tube. The reaction mixture was heated to 50 C and 2-fluorosulfonyl-2,2- difluoroacetic acid (15.0 g, 84.23 mmol) was added and stirred at 50 C at 18 h, then concentrated under reduced pressure at 30 C bath temperature. To the residue water (100 mL) was added and extracted with EtOAc (2 x 150 mL). The combined organic layers were washed with brine, dried (Na2S04), filtered and concentrated under reduced pressure at 30 C bath temperature which gave the title compound (1.1 g) as liquid. The compound was used in next step without further purification.

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route Methyl 1-hydroxycyclopropanecarboxylate, its application will become more common.

Reference:
Patent; MEDIVIR AKTIEBOLAG; ERSMARK, Karolina; KARLSTROeM, Sofia; KLASSON, Bjoern; LUNDGREN, Stina; ROSENQUIST, Asa; SALVADOR ODEN, Lourdes; (155 pag.)WO2018/226150; (2018); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Related Products of 426-65-3, Each compound has different characteristics, and only by selecting the characteristics of the compound suitable for a specific situation can the compound be applied on a large scale. 426-65-3, name is Ethyl Pentafluoropropionate, This compound has unique chemical properties. The synthetic route is as follows.

A solution of BOC protected aniline (14 g, 72 mmol) in anhydrous ether (150 mL) at -15 C. under nitrogen was treated with a solution of t-butyllithium (1.7 M in pentane, 106 mL, 183 mmol). The reaction mixture was stirred at -15 C. for 4 hrs, cooled to -78 C., and treated with ethyl pentafluoropropionate (13 mL, 88 mmol). The mixture was allowed to slowly warm to rt and brine (500 mL) was added. The organic layer was separated, dried (MgSO4), and concentrated. The residue was taken up in methylene chloride (100 mL) and treated with TFA (5 mL) at 0 C. under nitrogen. After 1.5 hrs, the solution was treated with a cold sodium bicarbonate solution (3N, 100 mL) and organic layer was separated, dried (MgSO4), and concentrated. The crude residue (5 g, 21 mmol) was then taken up in methylene chloride (80 mL) and treated with NBS (3.6 g, 20 mmol) in portions at rt under nitrogen. After 1 hr, the solution was washed with aqueous 3N sodium bicarbonate solution (3¡Á20 mL), dried (MgSO4), and concentrated to give 1-(2-amino-5-bromophenyl)-2,2,3,3,3-pentafluoropropan-1-one as a yellow solid (6 g, 25% in three steps). 1H NMR (DMSO-d6): delta 7.97 (s, 2H), 7.67 (d, J=2.3 Hz, 1H), 7.56 (dd, J=9.2, 2.2 Hz, 1H), 6.94 (d, J=9.3 Hz, 1H); MS (ESI) m/z 318/320 ([M+H]+); MS (ESI) m/z 316/318 ([M-H]-); Anal. calcd for C9H5BrF5NO: C, 33.99; H, 1.58; N, 4.40. Found: C, 34.27; H, 1.75; N, 4.22.

The chemical industry reduces the impact on the environment during synthesis Ethyl Pentafluoropropionate. I believe this compound will play a more active role in future production and life.

Reference:
Patent; Wyeth; US2005/215539; (2005); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Related Products of 58101-60-3, As we all know, there are many different methods for the synthesis of a compound, and people can choose the synthesis method that suits their own laboratory according to the actual situation. 58101-60-3 name is Methyl 3-cyclopentenecarboxylate, This compound is widely used in many fields, so it is necessary to find a new synthetic route. The downstream synthesis method of this compound is introduced below.

To a solution of N-methylmorpholine-N-oxide (2786 mg) in H20 (7 mL) and THF (19 mL) were added potassium osmate (VI) dihydrate (43.8 mg) in tBuOH (8 mL) and methyl 3- cyclopentenecarboxylate (1500 mg) under N2. The resulting mixture was stirred at rt overnight. The reaction mixture was treated with sodium bisulphite and extracted with DCM. The org. layer was washed with brine, dried over MgS04, filtered and concentrated under reduced pressure, affording a crude orange oil (1.39 g; 73% yield) which was used directly in the next step. 1H MR (CDC13) delta: 4.15-4.27 (m, 1H); 3.95-4.11 (m, 1H); 3.67 (s, 3H); 3.07-3.25 (m, 1H); 1.87-2.32 (m, 4H).

At the same time, in my other blogs, there are other synthetic methods of this type of compound, Methyl 3-cyclopentenecarboxylate, and friends who are interested can also refer to it.

Reference:
Patent; ACTELION PHARMACEUTICALS LTD; CREN, Sylvaine; FRIEDLI, Astrid; HUBSCHWERLEN, Christian; RUEEDI, Georg; ZUMBRUNN, Cornelia; WO2014/170821; (2014); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Adding a certain compound to certain chemical reactions, such as: 35065-86-2, name is 3-Bromophenyl acetate, belongs to esters-buliding-blocks compound, can increase the reaction rate and produce products with better performance than those obtained under traditional synthetic methods. Here is a downstream synthesis route of the compound 35065-86-2, Recommanded Product: 3-Bromophenyl acetate

Acetylated intermediate and aluminum trichloride (2.3g) with vigorous stirringThe mixture was heated to 160 C under an argon atmosphere for 2 h in a 50 mL single-mouth bottle, cooled to room temperature, and extracted with a 3 M hydrochloric acid solution and ethyl acetate.After the organic phase is washed with water and a saturated sodium chloride solution,Dry over anhydrous sodium sulfate.After concentration, column chromatography gave 1 g of pale yellow solid.

In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles, 3-Bromophenyl acetate, other downstream synthetic routes, hurry up and to see.

Reference:
Patent; Shanghai Changsen Pharmaceutical Co., Ltd.; Wang Zhe; Fan Guoqin; Zeng Zhihong; Wang Xiaoguang; Jiang Rongzhen; (64 pag.)CN109678796; (2019); A;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Reference of 103-26-4, A common heterocyclic compound, 103-26-4, name is Methyl cinnamate, molecular formula is C10H10O2, its traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc, below Introduce a new synthetic route.

6-methyl-4-phenyl-chromen-2-one (I ; X+Z=0 ; W = CO) 2-Bromo-4-methylphenol (2.4 ml ; 19.7 MMOL), ET4NCI (2.2 g; 13.3 MOI), CY2 (Me) N (4.2 ml ; 19.7 MMOL) and Pd (OAC) 2 (59 mg; 0.26 MMOL) were added under nitrogen at room temperature to a solution of methyl cinnamate (2.1 g; 13.1 MMOL) in DIMETHYLACETAMIDE (40 ML). The reaction mixture was stirred at 959C for 48 h, then cooled and filtered on celite. The solution was diluted with Et20 and washed 3 times with H20. The organic phase was dried over NA2SO4 and the solvent was evaporated under vacuum. GC-MS showed a conversion of 94%. The raw reaction product was purified by flash chromatography. (SIO2, n-hexane: Et20 7: 3) and the fractions collected were crystallized from ET20/N-HEXANE to give pale yellow crystals (2.4 g; 77% yield).

The synthetic route of 103-26-4 has been constantly updated, and we look forward to future research findings.

Reference:
Patent; CONSIGLIO NAZIONALE DELLE RICERCHE; PICCOLO, Oreste; WO2005/5356; (2005); A2;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Electric Literature of 4385-35-7, In the next few decades, the world population will flourish. As the population grows rapidly and people all over the world use more and more resources, all industries must consider their environmental impact. 4385-35-7, name is 3-Isochromanone belongs to esters-buliding-blocks compound, it is a common compound, a new synthetic route is introduced below.

Methyl 2-(2-(chloromethyl)phenyl)acetate. Hydrogen chloride gas was bubbled though a solution of 3-isochromanone (1.2 g, 8.1 mmol) in methanol (30 mL) for 3 minutes. Reaction stirred at room temperature for 8 hours. Mixture was diluted with water (70 mL). Mixture was extracted with dichloromethane (2¡Á40 mL). Combined organic layers were washed with brine (20 mL). Mixture was dried (magnesium sulfate), filtered and concentrated in vacuo. Title compound was obtained as clear colorless oil in 90% yield. 1H NMR (300 MHz, CDCl3): delta=7.40-7.26 (m, 4H), 4.67 (s, 2H), 3.80 (s, 2H), 3.69 (s, 3H).

In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles, 3-Isochromanone, other downstream synthetic routes, hurry up and to see.

Reference:
Patent; Chaturvedula, Prasad V.; Mercer, Stephen E.; Fang, Haiquan; US2006/94707; (2006); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics