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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495713Generated: October 29, 2026

Ammonium Chloride → 2-Chloro-5-vinyl-pyridine

https://huagongshe.com/reaction/495713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant6-Chloropyridine-3-carbaldehydeHCID 2764053—
ReactantPotassium tert-butoxideHCID 23665647—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
SolventTetrahydrofuranHCID 8028—
Product2-Chloro-5-vinyl-pyridineHCID 1181544361.7%

Reaction Conditions

Temperature5 °C

Reaction Steps

To a cooled (5° C.), stirred slurry of methyltriphenylphosphonium bromide (75.7 g) in tetrahydrofuran (530 mL) was added potassium t-butoxide (23.8 g) portionwise over a 5-min period to produce a yellow slurry. After 30 min, 2-chloro-5-formylpyridine (25.0 g) was added in one portion to produce a purple colored slurry. After an additional 30 min, the reaction mixture was treated with saturated aqueous ammonium chloride (200 mL) and a majority of the tetrahydrofuran was removed in vacuo. The resulting mixture was washed with ethyl acetate, the combined organic layers washed with saturated aqueous brine, stirred over activated charcoal for 20 min, dried over anhydrous sodium sulfate and concentrated in vacuo. The resulting semi-solid was stirred for 30 min with a solution of 2:1 diethyl ether/petroleum ether (375 mL), filtered and the solids washed with an additional portion of 2:1 diethyl ether/petroleum ether (300 mL). The combined filtrates were concentrated in vacuo, pre-loaded on 60 g of silica gel and chromatographed over 700 g of silica gel eluting with a gradient of ethyl acetate (0-8%)/hexanes to afford 15.2 g of the title compound (I-2b) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06939867B2
Source datasetuspto-grants-2005_09
ORD IDord-0c614a127d8746e2aced87bf4aa2e94e
Source noteuspto-grants-2005_09