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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1499116Generated: November 1, 2026

Ethyl trifluoroacetate → HCID 117942671, compound

https://huagongshe.com/reaction/1499116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl trifluoroacetateHCID 9794—
Reactant1-Bromo-4-chloro-2-(2-methoxyethoxy)benzeneHCID 53217041—
ReactantHCID 178418365HCID 178418365—
SolventTetrahydrofuranHCID 8028—
ProductHCID 117942671HCID 117942671—

Reaction Conditions

Temperature10 °C

Reaction Steps

1-Bromo-4-chloro-2-(2-methoxy-ethoxy)-benzene (CAS#1245563-20-5) (5.00 g, 18.8 mmol) was dissolved in THF (30 mL) and cooled to 0° C. i-Propylmagnesium bromide (11.3 mL, 2.0 M in THF, 22.6 mmol) was added dropwise, and the reaction was stirred at 10° C. for 30 min, then warmed to RT for 16 h. The reaction was then cooled to −15° C. and trifluoroacetic acid ethyl ester (3.37 mL, 28.2 mmol) was added. The reaction was stirred at 10° C. for 1 h. The reaction was quenched with HCl (2 N, 38 mL) at 0° C. The reaction mixture was diluted with water and extracted with EtOAc. The combined organic layers were washed with brine, dried over Na2SO4, then concentrated in vacuo. Purification by normal phase silica gel column chromatography (EtOAc/heptane) provided 1-(4-chloro-2-(2-methoxyethoxy)phenyl)-2,2,2-trifluoroethanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199994B2
Source datasetuspto-grants-2015_12
ORD IDord-552ca2c7f7b5462cbd5b71726b6a786f
Source noteuspto-grants-2015_12