HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847802Generated: October 25, 2026
Chloroform → 4-chloro-N-methylbenzothiazolone
https://huagongshe.com/reaction/847802
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | 4-Chloro-2-methoxybenzothiazole | HCID 4141969 | — |
| Product | 4-chloro-N-methylbenzothiazolone | HCID 69645010 | 99.7% |
Reaction Steps
A mixture of 4-chloro-2-methoxybenzothiazole (3.00 g, 0.015 mole) and dimethyl sulfate (95 mg, 7.5×10-4 mole) was heated at 150° C. for 3 hours with stirring. After cooling, the reaction mass was dissolved in chloroform, and the chloroform layer was washed with an aqueous solution saturated with sodium carbonate and then with water. The solvent was removed under reduced pressure to obtain 2.99 g of 4-chloro-N-methylbenzothiazolone as white crystals. Yield 99.7%, purity 99.0%, m.p. 130°-132° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04293702 |
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| Source dataset | uspto-grants-1981_10 |
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| ORD ID | ord-3430b6b0385643a59c87c7ea15694002 |
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| Source note | uspto-grants-1981_10 |
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