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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727290Generated: November 2, 2026

Chlorotrimethylsilane → Ethyl 2-bromo-2-(pyridin-3-yl)acetate

https://huagongshe.com/reaction/1727290

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantN-bromobutanimideHCID 67184—
ReactantEthyl 3-pyridylacetateHCID 96490—
ReactantLithium HexamethyldisilazideHCID 2733832—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-bromo-2-(pyridin-3-yl)acetateHCID 21985933—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Ethyl 3-pyridylacetate (1.0 g, 1.0 eq) was dissolved in THF (50 mL) and cooled to −78° C. Lithium bis (trimethylsilyl) amide (6.66 mL, 1.1 eq) was added to the reaction and stirred for 20 minutes. Chlorotrimethylsilane (1.44 mL, 1.875 eq) was added at −78° C. and stirred for 20 minutes. N-bromosuccinimide (1.09 g, 1.01 eq) was added to the reaction mixture. The reaction mixture was allowed to stir and warm to room temperature overnight. The reaction mixture was diluted with H2O. The organic layer was extracted with ethyl acetate. The organic phase was dried over sodium sulfate and the solvent was evaporated to give a yellow oil. The resulting oil was chromatographed on silica gel using hexanes and ethyl acetate (1:1) to give ethyl 2-bromo-2(3-pyridyl)acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07495020B2
Source datasetuspto-grants-2009_02
ORD IDord-fb8d7139865e42e18176f99840ce12f6
Source noteuspto-grants-2009_02