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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1717470Generated: November 2, 2026

Ethanol → Ethyl 3-chloro-5-trifluoromethoxyphenylacetate

https://huagongshe.com/reaction/1717470

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Chloro-5-(trifluoromethoxy)phenylacetic acidHCID 21904638—
CatalystSulfuric AcidHCID 1118—
ProductEthyl 3-chloro-5-trifluoromethoxyphenylacetateHCID 2190461896%

Reaction Steps

To a solution of 3-chloro-5-trifluoromethoxyphenylactic acid (5.2 g, 20.4 mmol; see step (iii) above) in EtOH (600 mL) was added sulfuric acid (several drops). The solution was refluxed for 18 h, cooled to room temperature, neutralized with solid NaHCO3 and the EtOH removed in vacuo. The residue was diluted with EtOAc then washed with H2O (1×), aqueous NaHCO3 (1×) and brine (1×). The organics were dried (Na2SO4), filtered and concentrated in vacuo to afford the sub-title compound (5.5 g, 96%) as an oil which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803954B2
Source datasetuspto-grants-2010_09
ORD IDord-cc36287251ee42a4a77e5dea4c05df77
Source noteuspto-grants-2010_09