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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474113Generated: October 25, 2026

Ethyl difluoroacetate → 1-(6-Bromo-3-fluoro-4-(triethylsilyl)pyridin-2-yl)-2,2-difluoroethanone

https://huagongshe.com/reaction/474113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl difluoroacetateHCID 9961—
ReactantLithium diisopropylamideHCID 2724682—
Reactant2-Bromo-5-fluoro-4-(triethylsilyl)pyridineHCID 86668068—
SolventTetrahydrofuranHCID 8028—
Product1-(6-Bromo-3-fluoro-4-(triethylsilyl)pyridin-2-yl)-2,2-difluoroethanoneHCID 8666808375%

Reaction Steps

To a freshly prepared solution of LDA (6.25 mmol) in THF (5 ml) was added dropwise a solution of 2-bromo-5-fluoro-4-triethylsilanylpyridine (1.6 g, 5.51 mmol) in THF (12 ml) at −78° C. Stirring was continued at −78° C. for 3 hours. Ethyl 2,2-difluoroacetate (0.58 ml, 5.51 mmol) was added dropwise and the solution was stirred at −78° C. for 3 hours. The reaction mixture was quenched with sat. ammonium chloride solution (20 ml) and ethyl acetate was added. The organic phase was washed with brine, dried over sodium sulfate, filtered and evaporated. The crude brown oil (2.11 g) was chromatographed over silica gel (cyclohexane/ethyl acetate) to give the title compound. 1.53 g (75% yield, mixture of ketone and hydrate form).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637508B2
Source datasetuspto-grants-2014_01
ORD IDord-8af69c0d2e084b30878654b5c5d26b4b
Source noteuspto-grants-2014_01