Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1869899Generated: October 30, 2026

Trifluoroacetic acid → HCID 57424237, compound

https://huagongshe.com/reaction/1869899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylsilaneHCID 12052—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 57424236HCID 57424236—
SolventWaterHCID 962—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
ProductHCID 57424237HCID 5742423753%

Reaction Conditions

Temperature55 °C

Reaction Steps

A solution of 4-(4-bromo-2-methoxy-phenyl)-4-oxo-butyric acid ethyl ester (Intermediate 60, 14.73 g, 46.8 mmol) in trifluoroacetic acid (72 mL, 935 mmol) was treated with triethylsilane (30 mL, 187 mmol) and the resulting reaction mixture was heated at 55° C. for 4 h. The reaction mixture was then cooled to ambient temperature, neutralized with solid sodium bicarbonate, diluted with water and extracted with diethyl ether. The organic phase was washed with water and brine, dried over anhydrous magnesium sulfate, filtered and evaporated in vacuo to afford a residue that was subjected to flash column chromatography over silica gel (230-400 mesh) using 8% ethyl acetate in hexane as the eluent to afford the title compound (7.4 g, 53%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07638648B2
Source datasetuspto-grants-2009_12
ORD IDord-3d06f96fbe6c4807a8951969722c57c0
Source noteuspto-grants-2009_12