Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552835Generated: October 26, 2026

1,3-Benzothiazole-6-carboxamide → Benzothiazole-6-carbonitrile

https://huagongshe.com/reaction/552835

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Benzothiazole-6-carboxamideHCID 43236343—
SolventPhosphorus oxychlorideHCID 24813—
ProductBenzothiazole-6-carbonitrileHCID 10607144—

Reaction Steps

A solution of 1,3-benzothiazole-6-carboxamide (1.96 g) in POCl3 (10 ml) was refluxed for 4 hours. The reaction solution was concentrated, and water was slowly added thereto at 0° C. It was extracted with EtOAc, and the organic layer was dried over anhydrous MgSO4, and then filtered, and the filtrate was concentrated. The residue was purified by silica gel column chromatography (n-hexane:EtOAc=80:20 to 60:40) to obtain 1,3-benzothiazole-6-carbonitrile as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07951825B2
Source datasetuspto-grants-2011_05
ORD IDord-241cd22099eb4a6b867cd58491a17d1e
Source noteuspto-grants-2011_05