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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604639Generated: October 30, 2026

Thionyl Chloride → 2-(4-Tert-butylthiazol-2-yl)benzofuran-5-carbonyl chloride hydrochloride

https://huagongshe.com/reaction/1604639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant2-(4-Tert-butylthiazol-2-yl)benzofuran-5-carboxylic acidHCID 19603694—
SolventTetrahydrofuranHCID 8028—
Product2-(4-Tert-butylthiazol-2-yl)benzofuran-5-carbonyl chloride hydrochlorideHCID 19603831—

Reaction Steps

A solution of 2-(4-tert-butylthiazol-2-yl)benzofuran-5-carboxylic acid (5.0 g) and thionyl chloride (12.1 ml) in tetrahydrofuran (50 ml) was stirred at 50° C. for 2 hours. After the solution was cooled to room temperature, the resulting precipitates were collected by filtration and washed with diisopropyl ether to give 2-(4-tert-butylthiazol-2-yl)benzofuran-5-carbonyl chloride hydrochloride (5.57 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05994378
Source datasetuspto-grants-1999_11
ORD IDord-648fb067932a4e0b92fd92299ea25dda
Source noteuspto-grants-1999_11