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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35459Generated: October 29, 2026

Trichloroacetyl chloride → 2-Chloromethyl-4-tert-butyl-3-methylpyridine

https://huagongshe.com/reaction/35459

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloroacetyl chlorideHCID 6420—
ReactantSodium BicarbonateHCID 516892—
Reactant4-tert-butyl-2,3-dimethylpyridine N-oxideHCID 53658474—
SolventChloroformHCID 6212—
Product2-Chloromethyl-4-tert-butyl-3-methylpyridineHCID 21295957—

Reaction Steps

A solution of 9.8 g of 4-tert-butyl-2,3-dimethylpyridine N-oxide in 120 ml of abs. chloroform is boiled at reflux under argon and treated through the condenser with 25.5 ml of trichloroacetyl chloride. After 22 hours the reaction mixture is poured on to ice, whereupon 10% sodium bicarbonate solution is added, the mixture is extracted with methylene chloride and the methylene chloride solution is dried and concentrated. The thus-obtained crude product is chromatographed on silica gel (solvent: methylene chloride/ether [10:1]). The 2-chloromethyl-4-tert-butyl-3-methylpyridine obtained is processed directly.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04766133
Source datasetuspto-grants-1988_08
ORD IDord-e812e4ec5734406e872ef7293d6f9d85
Source noteuspto-grants-1988_08