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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23757Generated: October 26, 2026

(Diethylamino)sulfur trifluoride → 4,4-Difluoro-4-(4'-methoxy-biphenyl-4-yl)-butyric Acid

https://huagongshe.com/reaction/23757

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Diethylamino)sulfur trifluorideHCID 123472—
ReactantEthyl α,α-difluoro-4′-methoxy[1,1′-biphenyl]-4-acetateHCID 46220012—
ReactantHCID 69784836HCID 69784836—
SolventDichloromethaneHCID 6344—
Product4,4-Difluoro-4-(4'-methoxy-biphenyl-4-yl)-butyric AcidHCID 9839508—

Reaction Steps

Difluoro-(4′-methoxy-biphenyl-4-yl)-acetic acid ethyl ester. Diethylaminosulfur trifluoride (5 mL) is added directly to (4′-methoxy-biphenyl-4-yl)-oxo-acetic acid ethyl ester (3.77 g, 13.3 mmol), prepared as described by Neidlin, et. al., Arzneim.-Forsch. 1983, 33, 691-3. Dichloromethane (2 mL) is added and the mixture is stirred overnight at room temperature. The reaction is diluted with dichloromethane and slowly added to ice water. This mixture is extracted with ethyl acetate twice. The combined organic extracts are dried over Na2SO4, filtered, and concentrated under reduced pressure. The crude product is purified by column chromatography (silica gel, 5% EtOAc/hexanes) to give the desired product as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06852751B2
Source datasetuspto-grants-2005_02
ORD IDord-e8ca589573444b1b96f7b6fcfff3247d
Source noteuspto-grants-2005_02