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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 344709Generated: October 26, 2026

Methyl iodide → 5-Chloro-2-(methylthio)benzothiazole

https://huagongshe.com/reaction/344709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 178527796HCID 178527796—
SolventDimethylformamideHCID 6228—
Product5-Chloro-2-(methylthio)benzothiazoleHCID 64574698.1%

Reaction Steps

With stirring under ice cooling, 2.00 g (9.92 mmols) of 5-chloro-2-mercaptobenzothiazole was added gradually to 10 ml of a solution of 0.24 g (10.00 mmols) of sodium hydroxide in dimethylformamide (DMF). The mixture was dropwise added to 20 ml of a solution of 0.62 ml (9.96 mmols) of iodomethane in 20 ml of DMF with stirring under ice cooling and the mixture was stirred for further 30 minutes under ice cooling. The mixture was concentrated under reduced pressure, and to the residue was added an aqueous saturated sodium bicarbonate followed by extraction of the solution with chloroform. The chloroform layer was dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: chloroform/methanol =100/1) to afford 2.10 g (yield: 98%) of 5-chloro-2-methylthiobenzothiazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05053408
Source datasetuspto-grants-1991_10
ORD IDord-042dce2aab6841d0a8823b8c8bcc9c6c
Source noteuspto-grants-1991_10