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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656806Generated: October 26, 2026

Methyl alpha-phenylbenzeneacetate → Methyl 2-fluoro-2,2-diphenylacetate

https://huagongshe.com/reaction/1656806

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl alpha-phenylbenzeneacetateHCID 77019—
ReactantN-FluorobenzenesulfonimideHCID 588007—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 2-fluoro-2,2-diphenylacetateHCID 1322256882%

Reaction Steps

4.8 milliliters KN(SiCH3)2 were dropped into 5 milliliters (C6H5)2CHCOOCH3 in tetrahydrofuran at -78° C. and the resulting yellow suspension was stirred for 45 minutes. 1.2 molar equivalents N-fluorobenzenesulfonimide prepared according to Example 1 above in 4 milliliters tetrahydrofuran were dropped into the mixture and stirring continued at -78° C. for 1 hour. The mixture was allowed to warm up to room temperature, quenched with ammonium chloride, and acidified with 0.1N hydrogen chloride. Extraction with dichloromethane, drying, and evaporation were followed by purification on a silica gel column. White crystalline (C6H5)2CFCOOCH3 was obtained in 82% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05254732
Source datasetuspto-grants-1993_10
ORD IDord-f22a2215997a4cb2adf2976ebed4cca1
Source noteuspto-grants-1993_10