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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349390Generated: November 1, 2026

4-Toluenesulfonyl chloride → HCID 86602193, compound

https://huagongshe.com/reaction/349390

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
ReactantHCID 86602191HCID 86602191—
SolventChloroformHCID 6212—
ProductHCID 86602193HCID 8660219370.1%

Reaction Steps

2-Bromomethyl-5-ethoxy-carbonyl-4-hydroxy-thiazole (8 g, 0.03 mol) was dissolved in 80 ml of chloroform. The solution was then cooled down to 0° C. p-Toluenesulfonyl chloride (5.7 g, 0.03 mol) was added, followed by slow addition of triethylamine (3.64 g, 0.036 mol) at 0° C. The reaction was monitored by TLC and LCMS. After the reaction was done, solvent was evaporated and the crude product was then purified by column chromatography to give 8.5 g of title product (yield 67%; LC: Retention Time=2.05 min; MS: M+1=421).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179827B2
Source datasetuspto-grants-2007_02
ORD IDord-f08f2686ab1543b699603a59a5a40a8f
Source noteuspto-grants-2007_02