Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234783Generated: October 30, 2026

Benzoyl chloride → 3-(Benzoyloxy)-4-methyl-1,3-thiazole-2(3H)-thione

https://huagongshe.com/reaction/234783

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
Reactant3-Hydroxy-4-methyl-2(3H)-thiazolethioneHCID 341593—
ReactantSodium BicarbonateHCID 516892—
SolventWaterHCID 962—
Product3-(Benzoyloxy)-4-methyl-1,3-thiazole-2(3H)-thioneHCID 23355623—

Reaction Steps

0.735 parts of 3-hydroxy-4-methylthiazol-2(3H)-thione were stirred in 50 parts of water and 0.84 parts of sodium hydrogen carbonate. The solution was screened and 0.9 parts of benzoyl chloride were added. The reaction mixture was stirred overnight at room temperature. A precipitate was formed which was separated by filtration, washed with cold water and recrystallised from ethanol to give 3-benzoyloxy-4-methylthiazol-2(3H)-thione, m.pt. 100°-102° C. By analysis the composition was found to be C 52.4% wt; H 3.6% wt; N 5.6% wt and S 25% wt. C11H9NO2S2 requires C 52.6% wt; H 3.6% wt; N 5.6% wt and S 25.5% wt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05596102
Source datasetuspto-grants-1997_01
ORD IDord-5f57f49aa6a847d080a6a57537929bd9
Source noteuspto-grants-1997_01