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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl 2-chloro-4-methylbenzo[d]thiazole-5-carboxylate | HCID 22390080 | — |
| Reactant | Potassium methoxide | HCID 23664618 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 5-Benzothiazolecarboxylic acid,2,3-dihydro-4-methyl-2-oxo-,methyl ester | HCID 22390075 | 55% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06908884B2 |
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| Source dataset | uspto-grants-2005_06 |
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| ORD ID | ord-7b28043bae3a4d7f827f761c5a82f3ac |
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| Source note | uspto-grants-2005_06 |
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