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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2165991Generated: November 4, 2026

Benzyl mercaptan → 2-(Benzylsulfanyl)-4-chloro-1,3-thiazole

https://huagongshe.com/reaction/2165991

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl mercaptanHCID 7509—
ReactantSodiumHCID 5360545—
ReactantSodium MethoxideHCID 10942334—
Reactant2,4-DichlorothiazoleHCID 12333155—
SolventEthanolHCID 702—
Product2-(Benzylsulfanyl)-4-chloro-1,3-thiazoleHCID 1507711890.7%

Reaction Steps

Benzylmercaptan (24.8 g) was added dropwise to a solution of 10.8 of sodium methoxide in 100 ml ethanol. After stirring 15 minutes, the ethanolic solution of sodium benzylmercaptide was added dropwise to a solution of 30.8 g 2,4-dichlorothiazole [prepared by the method of P. Reynaud et al., Bull. Soc. Chim. France, 1735 (1962)], resulting in a temperature increase of 28° to 48°. When the exotherm subsided, the suspension was refluxed 1 hour, then the solvent was evaporated. Cold water (300 ml) was added to the oily residue, and the aqueous mixture was extracted with methylene chloride. The organic solution was washed with water, followed by saturated brine, then dried over magnesium sulfate, filtered and the solvent evaporated to give 43.8 g of 4-chloro-2-phenylmethylthiothiazole as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04943312
Source datasetuspto-grants-1990_07
ORD IDord-486820994f1c469ca0b5de720c35398e
Source noteuspto-grants-1990_07