Esters-buliding-blocks

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. 251458-15-8, name is Methyl 2-(3-bromophenyl)-2-methylpropanoate, A new synthetic method of this compound is introduced below., COA of Formula: C11H13BrO2

To a solution of ester from step 1 in THF-MeOH (4: 1,0. 5M) was added LIOH (3 eq, 2M) and the mixture was stirred at 50C for 1h. The organic solvent evaporated, aqueous was acidified with HCl IN and the acid extracted with EtOAc (3X). The organic was washed with brine, dried and solvent evaporated to afford the acid.

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; MERCK FROSST CANADA & CO.; WO2004/48374; (2004); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Reference of 56441-97-5, 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. 56441-97-5, name is Methyl 4-(benzyloxy)-3-methoxybenzoate belongs to esters-buliding-blocks compound, it is a common compound, a new synthetic route is introduced below.

REFERENCE EXAMPLE 15 Methyl 5-methoxy-2-nitro-4-(benzyloxy) benzoate Nitric acid (27 mL of a 70% solution) was added dropwise to a suspension of methyl 3-methoxy-4-(benzyloxy) benzoate (14.5 g, 53.0 mmol) in 150 mL of acetic acid. The mixture was stirred at room temperature for 15 minutes and then was heated at 50 C. for 4 hours. The reaction was cooled to room temperature and poured into ice. The precipitate was collected by filtration, washed with water and dried to provide 16.4 g of methyl 5-methoxy-2-nitro-4-(benzyloxy) benzoate as an off-white solid, mp 104-105 C.; MS (ES) m/z 318.1 (M+1). Analysis for C16H15NO6: Calcd: C, 60.57;H, 4.76; N, 4.41. Found: C, 60.39;H, 4.70; N, 4.28.

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, Methyl 4-(benzyloxy)-3-methoxybenzoate, other downstream synthetic routes, hurry up and to see.

Reference:
Patent; American Home Products Corporation; US2002/26052; (2002); 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. 72338-48-8, name is Ethyl 12-bromododecanoate, This compound has unique chemical properties. The synthetic route is as follows., COA of Formula: C14H27BrO2

c) Synthesis of ethyl 13-(diethoxyphosphoryl)tridecanoate In a single-neck flask with a reflux condenser, ethyl 12-bromododecanoate is weighed (1.8 g, 7.37 mmol) and triethyl phosphite (2.6 mL, 15 mmol) is added. The reaction mixture is brought to 150C and left stirring under a static head of nitrogen. After 24 hours the one neck balloon is attached to the high vacuum pump to eliminate volatile products and the resulting dense oil is directly loaded with column chromatography on silica gel. It is eluted with a mixture of ethyl acetate/petroleum ether 1/1 which leads to the isolation of 2.5 g (yield 94%) of ethyl 13-(diethoxyphosphoryl)tridecanoate as a colourless oil.

According to the analysis of related databases, 72338-48-8, the application of this compound in the production field has become more and more popular.

Reference:
Patent; Colorobbia Italia S.p.a.; EP1979365; (2012); B1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Application of 927-68-4, The chemical industry reduces the impact on the environment during synthesis 927-68-4, name is 2-Bromoethyl acetate, I believe this compound will play a more active role in future production and life.

Step 14b. 2-(6-Amino-8-(6-iodobenzo[d][1,3]dioxol-5-ylthio)-9H-purin-9-yl)ethyl acetate (Compound 401-38); A mixture of compound 105-38 (3.89 g, 9.41 mmol), Cs2CO3 (3.68 g, 11.3 mmol), 2-bromoethyl acetate (1.89 g, 11.3 mmol) and anhydrous DMF (50 mL) was stirred for 2 h at 50 C. The solvent was removed under high vacuum and the crude purified by column chromatography on silica gel (CH2Cl2/MeOH=60/1) to provide target compound 401-38 as a pale yellow solid (2.95 g, 62.8%): LCMS: 500 [M+1]+.

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, 2-Bromoethyl acetate, other downstream synthetic routes, hurry up and to see.

Reference:
Patent; Qian, Changgeng; Cai, Xiong; Gould, Stephen; Zhai, Haixiao; US2008/234297; (2008); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Synthetic Route of 369-26-6, These common heterocyclic compound, 369-26-6, name is Methyl 3-amino-4-fluorobenzoate, 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.

HATU (116 mg, 0.305 mmol) was added to picolinic acid (37.5 mg, 0.305 mmol) and DIPEA (66 mu, 0.381 mmol) in DMF (2 ml). After 15 min, methyl 3-amino-4-fluorobenzoate (43 mg, 0.254 mmol) in DMF (1 ml) was added. The mixture was stirred at ambient temperature for 10 d before solvent was evaporated and residue dissolved in EtOAc. The solution was washed with sat. NaHC03, dried (MgS04) and evaporated. Half of the crude material from above (0.127 mmol) was dissolved in dioxane (1.5 ml) and MeCN (1.5 ml). Potassium carbonate (35 mg, 0.254 mmol) was added and the mixture was heated at 180 ¡ãC for 2 h in a microwave reactor. Silica gel was added and solvents evaporated. The dry silica was applied on a flash column which was eluted with 35-50percent) EtOAc in hexanes. Yield: 6 mg (18percent>); colourless oil.

Statistics shows that Methyl 3-amino-4-fluorobenzoate is playing an increasingly important role. we look forward to future research findings about 369-26-6.

Reference:
Patent; KANCERA AB; HAMMER, Kristin; JOeNSSON, Mattias; KRUeGER, Lars; (230 pag.)WO2017/108282; (2017); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

3196-15-4, name is Methyl 2-bromobutyrate, belongs to esters-buliding-blocks compound, is considered to be a conventional heterocyclic compound, which is widely used in drug synthesis. The chemical synthesis route is as follows. Product Details of 3196-15-4

General procedure: As part of this general procedure, the appropriate diphenyl diselenide (9.5 mmol) dissolved in a 1:1 mixture of water and THF (50 mL) underprotective nitrogen gas, sodiumborohydride (47.5 mmol) was added and the mixture was stirred for around 35 minutes while observing adecolorization in the first 1-3 minutes. Next, a solution of a methyl -2-bromo-acetate derivatives (19.37 mmol) in THF or DCM (5 mL) wasadded and the reaction was stirred at room temperature and monitored via thin layer chromatography (TLC). Upon consumption of the startingmaterial usually occuring after 24-48 hours, the reaction mixture was diluted with 50 mL of a saturated aqueous solution of ammoniumchloride and extracted with diethyl ether. The combined organic extracts dried over sodium sulfate, and the solvent was evaporated under reducedpressure to obtain the desired intermediate, which was used without further purification.

The synthetic route of 3196-15-4 has been constantly updated, and we look forward to future research findings.

Reference:
Article; Ali, Wesam; Battistelli, Cecilia; D?browska, Monika; Handzlik, Jadwiga; Honkisz-Orzechowska, Ewelina; Jacob, Claus; Kincses, Annamaria; Latacz, Gniewomir; Nove, Marta; Rasile, Manuela Monica; Romanelli, Annalisa; Spengler, Gabriella; Starek, Ma?gorzata; Szyma?ska, Ewa; Zwergel, Clemens; European Journal of Medicinal Chemistry; vol. 200; (2020);,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

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. 454-31-9, name is Ethyl 2,2-difluoroacetate belongs to esters-buliding-blocks compound, it is a common compound, a new synthetic route is introduced below. Application In Synthesis of Ethyl 2,2-difluoroacetate

0 g of (1R,2S)-2-amino-1-(4-chlorophenyl)-3-fluoropropan-1-ol was dissolved in 350ml_ methanol, and then 5g of triethyl amine and 30.5g of ethyl difluoroacetate were added and stirred for 12 hours at room temperature. The solvent was evaporated off under reduced pressure, and the residue was recrystallized in isopropanol and water to obtain 12.7g of a white solid (yield 92%).

The synthetic route of 454-31-9 has been constantly updated, and we look forward to future research findings.

Reference:
Patent; ZOETIS SERVICES LLC.; DEJONG, Randall Lee; KARRICK, Gregory Lee; STUK, Timothy Lee; (56 pag.)WO2020/68607; (2020); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Related Products of 56441-97-5,Some common heterocyclic compound, 56441-97-5, name is Methyl 4-(benzyloxy)-3-methoxybenzoate, molecular formula is C16H16O4, 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.

4.1.4 Methyl 4-benzyloxy-5-methoxy-2-nitrobenzoate (12) To a suspension of intermediate 11 (10.1 g, 37 mmol) in AcOH (100 mL) was slowly added 70% HNO3 (20 mL). Subsequently, the mixture was heated to 50 C for 5 h, then cooled to room temperature and poured into ice water (500 mL). After stirring for 1 h, the resulting precipitate was filtered off, washed with water and dried to obtain the nitro compound 12 as a white solid. Yield: 86%, mp: 126-128 C.

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route Methyl 4-(benzyloxy)-3-methoxybenzoate, its application will become more common.

Reference:
Article; Cheng, Weiyan; Yuan, Youting; Qiu, Ni; Peng, Peng; Sheng, Rong; Hu, Yongzhou; Bioorganic and Medicinal Chemistry; vol. 22; 24; (2014); p. 6796 – 6805;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Adding a certain compound to certain chemical reactions, such as: 252881-74-6, name is tert-Butyl 3-(2-(2-(2-aminoethoxy)ethoxy)ethoxy)propanoate, 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 252881-74-6, Product Details of 252881-74-6

Example 32Step 1: ( 15R,19R)-tert-butyl 15-(((( 9H-fluoren-9-yl)methoxy)carbonyl)amino)-19-( dodecyloxy)-14- oxo-4, 7, 10,21 -tetraoxa-17-thia-13-azatritriacontan-l-oate[000538] To a solution of (?)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(((?)-2,3- bis(dodecyloxy)propyl)thio)propanoic acid (1 eq, from example 20, step 5) and HBTU (1.2 eq) inDCM (0.06 M) was added DIEA (3.5 eq), followed by teri-butyl 3-(2-(2-(2- aminoethoxy)ethoxy)ethoxy)propanoate (1.2 eq). The reaction was stirred at room temperature for2 hours. The crude mixture was purified by flash chromatography on a COMBIFLASH system(ISCO) using 0-5% MeOH/DCM to give the title product as a white solid.

At the same time, in my other blogs, there are other synthetic methods of this type of compound, tert-Butyl 3-(2-(2-(2-aminoethoxy)ethoxy)ethoxy)propanoate, and friends who are interested can also refer to it.

Reference:
Patent; IRM LLC; WU, Tom Yao-Hsiang; ZOU, Yefen; HOFFMAN, Timothy Z.; PAN, Jianfeng; WO2011/119759; (2011); 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. 82702-31-6, name is Methyl 3-bromo-4-fluorobenzoate, A new synthetic method of this compound is introduced below., Safety of Methyl 3-bromo-4-fluorobenzoate

Cesium carbonate (3.1 g, 9.6 mmol) was added to 4-fluoro-2,6-dimethylphenol (0.9 g, 6.4 mmol) and methyl 3-bromo-4-fluorobenzoate (1.57 g, 6.7 mmol) ) in a solution of dimethyl sulfoxide (10 mL). The reaction mixture was stirred at 80 C for 12 hr, then cooled to room temperature, then water (50mL), ethyl acetate (50mL*2). The organic phase was washed with brine (25 mL*4) and evaporated to dryness. The crude product was separated by column ( petroleum ether: ethyl acetate = 20:1) to give methyl 3-bromo-4-(4-fluoro-2,6-dimethylphenoxy) benzoate (1.4 g, 3.97 mmol , molar yield 62%).

The synthetic route of 82702-31-6 has been constantly updated, and we look forward to future research findings.

Reference:
Patent; Shanghai Hansen Bio-pharmaceutical Technology Co., Ltd.; Jiangsu Haosen Pharmaceutical Group Co., Ltd.; Sun Changan; Zhang Xiaoyu; Chen Gangsheng; Zong Shumin; (45 pag.)CN109836385; (2019); A;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics