Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339490Generated: October 29, 2026

Benzothiazole → HCID 178511489, compound

https://huagongshe.com/reaction/339490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzothiazoleHCID 7222—
ReactantSodium HydroxideHCID 14798—
ReactantThiobenzamideHCID 683563—
ReactantHCID 178511488HCID 178511488—
SolventWaterHCID 962—
ProductHCID 178511489HCID 178511489—

Reaction Conditions

Temperature5 °C

Reaction Steps

In this reaction, a thiobenzamide is converted to a benzothiazole in the presence of potassium ferricyanide. In a typical reaction, a thiobenzamide (1 equiv) is dissolved in NaOH (1.5 M, 39 equiv.) and the solution cooled to 5° C. with ice. Potassium ferricyanide in water (20%, 15 vol) is added and the reaction stirred at it for 18 h. The mixture is filtered and the solid washed with H2O. The solid is dissolved in DCM (20 vol), dried (Na2SO4) and the solvent removed under reduced pressure to give the crude benzothiazole product. Column chromatography may be carried out in order to obtain the pure target material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895313B2
Source datasetuspto-grants-2014_11
ORD IDord-020593f2c3df42c3995f170760703ab1
Source noteuspto-grants-2014_11