HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 4703Generated: October 29, 2026
Acetic Acid → Benzothiazole, 6-chloro-2-methyl-
https://huagongshe.com/reaction/4703
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 4-Chloro-2-mercaptophenylurea | HCID 21274148 | — |
| Solvent | Water | HCID 962 | — |
| Product | Benzothiazole, 6-chloro-2-methyl- | HCID 138133 | 93.3% |
Reaction Steps
112.25 parts of the sodium salt of 4-chloro-2-mercaptophenylurea, which salt is obtainable according to Example 6 of European Pat. No. 0,039,483, are suspended in 450 parts of glacial acetic acid in an autoclave. The pressure vessel is closed and heated slowly to 150° C.-160° C. in the course of 2 hours, a pressure of about 5 bar being established. The water formed is discharged continuously via a pressure release valve. The reaction is complete after 5 hours. The autoclave is cooled to room temperature and opened, the reaction mixture is allowed to run into 1000 parts of water, and the precipitated 6-chloro-2-methylbenzothiazole is isolated by filtration, washed neutral and dried in vacuo at 40° C. 85.6 parts of a product of the formula ##STR21## of melting point 85° C.-86° C. are obtained; this corresponds to a yield of 93.3% of theory, based on sodium salt employed.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04727154 |
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| Source dataset | uspto-grants-1988_02 |
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| ORD ID | ord-933065a153024599baa544ac59e11817 |
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| Source note | uspto-grants-1988_02 |
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