Continuously updated synthesis method about 2967-66-0

The chemical industry reduces the impact on the environment during synthesis Methyl 4-(trifluoromethyl)benzoate. I believe this compound will play a more active role in future production and life.

Electric Literature of 2967-66-0, 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. 2967-66-0, name is Methyl 4-(trifluoromethyl)benzoate, This compound has unique chemical properties. The synthetic route is as follows.

Several other esters, whose structure and names are described in Table 3, were hydro genated under the conditions described above using preformed RuCl2(L-I). Isolated yield are given in Table 4.Table 3: Structure and names of substrates usedTable 4: Hydrogenation of esters using RuCl2(L-I) EPO Sub.: Substrate as described in Table 3.Conv.: Conversion (in %, analysed by GC after silylation) of ester to alcohol after 2h30min.Reaction conditions: Substrate (20 mmol), H2 gas (50 bars), RuCl2(L-I) 0.05 mol%,NaOMe 10 mol%, THF (14 mL) at 1000C during 2h 30min.

The chemical industry reduces the impact on the environment during synthesis Methyl 4-(trifluoromethyl)benzoate. I believe this compound will play a more active role in future production and life.

Reference:
Patent; FIRMENICH SA; WO2006/106484; (2006); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics