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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333766Generated: October 27, 2026

Triethylamine → 2-Chloro-4-(trifluoromethyl)-benzeneacetic acid methyl ester

https://huagongshe.com/reaction/333766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Chloro-4-trifluoromethylphenylacetic acidHCID 12088185—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product2-Chloro-4-(trifluoromethyl)-benzeneacetic acid methyl esterHCID 5747405394.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-Chloro-4-(trifluoromethyl)-benzeneacetic acid (3 g) [CAS Reg. No. 601513-26-2] was dissolved in DCM (30 mL) and methyl chloroformiate (1.18 g, 0.97 mL) followed by triethylamine (1.4 g, 1.93 mL) were added drop by drop. To the mixture was added DMAP (0.154 g) and the yellow mixture was allowed to stir for 1 hour at 0° C. A clear solution was obtained. The mixture was diluted with DCM (30 mL) and was poured into sat. NH4Cl solution. The layers were separated and the aqueous phase was further extracted with 2 portions of DCM. The organic layers were washed with brine, dried over Na2SO4 and evaporated to give the title compound (3.0 g) that was used without further purification. NMR, (CDCl3): 7.6-7.4 (m, 3H); 3.84 (s, 2H); 3.74 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883786B2
Source datasetuspto-grants-2014_11
ORD IDord-3f49432e722541b0a187816e3371d5be
Source noteuspto-grants-2014_11