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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1071906Generated: November 1, 2026

Methyl 2-chloro-4-methylbenzo[d]thiazole-5-carboxylate → 5-Benzothiazolecarboxylic acid,2,3-dihydro-4-methyl-2-oxo-,methyl ester

https://huagongshe.com/reaction/1071906

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 2-chloro-4-methylbenzo[d]thiazole-5-carboxylateHCID 22390080—
ReactantPotassium methoxideHCID 23664618—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product5-Benzothiazolecarboxylic acid,2,3-dihydro-4-methyl-2-oxo-,methyl esterHCID 2239007555%

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of 22.5 g (93 mmol) of methyl 2-chloro-4-methyl-benzothiazole-5-carboxylate in 360 ml of N-methylpyrrolidone was admixed with 13.6 g (186 mmol) of potassium methoxide and heated at 100° C. for 5 hours. After cooling, the resulting precipitate was filtered off with suction and the filtrate was admixed with water. The pH of the reaction solution was then adjusted to pH 1, the aqueous solution was extracted three times with ethyl acetate and the combined organic phases were washed and dried. The solvent was removed under reduced pressure and the residue was purified by trituration with methylene chloride/n-hexane. This gave, in a yield of 55%, 11.38 g (51 mmol) of methyl 4-methylbenzothiazol-2-one-5-carboxylate of m.p. 262° C.-266° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06908884B2
Source datasetuspto-grants-2005_06
ORD IDord-7b28043bae3a4d7f827f761c5a82f3ac
Source noteuspto-grants-2005_06