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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2073693Generated: October 31, 2026

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

https://huagongshe.com/reaction/2073693

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl mercaptanHCID 7509—
ReactantSodium MethoxideHCID 10942334—
Reactant4-Chloro-1,3-thiazoleHCID 13517394—
SolventEthanolHCID 702—
Product4-(Benzylsulfanyl)-1,3-thiazoleHCID 1507712037.8%

Reaction Conditions

Temperature65 °C

Reaction Steps

Benzylmercaptan (24.8 g) was added slowly to a solution of 10.8 g of sodium methoxide in 100 ml ethanol. After 10 minutes, the reaction mixture was heated to 65° C. and a solution of 23.8 g of 4-chlorothiazole [prepared by the method of P. Reynaud et al., Bull. Soc. Chim. France, 1735 (1962)] in 25 ml ethanol was added dropwise. When addition was complete, the reaction mixture was refluxed 36 hours. The reaction mixture was cooled, and the bulk of the solvent evaporated. Cold water (300 ml) was added to the residue, and the aqueous mixture was extracted with 200 ml ether followed by 200 ml methylene chloride. The combined organic solution was washed with brine, dried over magnesium sulfate, filtered and the solvent evaporated. Distillation of the resulting yellow oil gave 15.6 g of 4-(phenylmethylthio)thiazole, bp 122-134 (0.6 mm).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04919706
Source datasetuspto-grants-1990_04
ORD IDord-bbed34baa8114ff89f3a5ec24279a3aa
Source noteuspto-grants-1990_04