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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1760736Generated: October 31, 2026

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

https://huagongshe.com/reaction/1760736

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 11815443—

Reaction Steps

To a cooled 5° C., stirred slurry of methyltriphenylphosphonium bromide (75.7 grams) in tetrahydrofuran (530 mL) was added potassium t-butoxide (23.8 grams) portionwise over a 5 minute period to produce a yellow slurry. After 30 minutes, 2-chloro-5-formylpyridine (25.0 grams) was added in one portion to produce a purple colored slurry. After an additional 30 minutes, 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 minutes, dried over anhydrous sodium sulfate and concentrated in vacuo. The resulting semi-solid was stirred for 30 minutes 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 grams of silica gel and chromatographed over 700 grams of silica gel eluting with a gradient of ethyl acetate(0-8%)/hexanes to afford the title compound as a colorless oil, 15.2 grams 1H NMR (400 MHz, CDCl3): δ=8.35 (s, 1H); 7.69(d,1H); 6.65 (dd, 1H); 5.79 (d, 1H);5.40 (d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06844441B2
Source datasetuspto-grants-2005_01
ORD IDord-8bf35066d21b4779a0fa7c65ac1ee5cf
Source noteuspto-grants-2005_01