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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2358145Generated: November 1, 2026

Water → 1-(3-Bromo-2-fluorophenyl)-2,2,2-trifluoroethan-1-one

https://huagongshe.com/reaction/2358145

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl trifluoroacetateHCID 9794—
Reactant1-Bromo-2-fluorobenzeneHCID 61259—
ReactantLithium diisopropylamideHCID 2724682—
SolventTetrahydrofuranHCID 8028—
Product1-(3-Bromo-2-fluorophenyl)-2,2,2-trifluoroethan-1-oneHCID 6753286630.7%

Reaction Steps

To a solution of 1-bromo-2-fluorobenzene (5.0 g, 28.6 mmol) in dry tetrahydrofuran (50 ml) under nitrogen, at −78° C. was added lithium diisopropylamide (2.0 M in hexane, 15.7 ml, 31.4 mmol). The mixture was stirred for 5 minutes after which ethyl trifluoroacetate (3.76 ml, 31.4 mmol) was added and the stirring was continued at −78° C. for an additional hour. The reaction mixture was brought to ambient temperature and water (50 ml) was added. The phases were separated and the aqueous phase extracted with ethylacetate (3×100 ml). The combined organic phases was dried (MgSO4) and evaporated to dryness to give an oil. The residue was purified by flash column chromatography (isooctane) to give the title compound (2.38 g). MS m/z (relative intensity, 70 eV) 272 (M+, 11), 270 (M+, 11), 203 (97), 201 (bp, 173 (46).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07763639B2
Source datasetuspto-grants-2010_07
ORD IDord-ffe8ab06bf8145719fd2d2509ec6b97d
Source noteuspto-grants-2010_07