HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1288532Generated: October 26, 2026
O-Ethyl carbamothioate → 2-Hydroxy-5,6-dihydro-4H-benzothiazol-7-one
https://huagongshe.com/reaction/1288532
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | O-Ethyl carbamothioate | HCID 3032339 | — |
| Reactant | 2-Chloro-1,3-cyclohexanedione | HCID 13483328 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Hydroxy-5,6-dihydro-4H-benzothiazol-7-one | HCID 6424598 | 36.1% |
Reaction Steps
A mixture of 29.3 g of 2-chloro-1,3-cyclohexanedione [Muehlstaedt et al, J. Prakt Chem., Vol. 20 (1963), p. 285] and 21 g of ethyl thiocarbamate was heated at 140° C for 15 minutes and was then poured into water. The precipitate formed was recovered by vacuum filtering and was crystallized from isopropyl alcohol to obtain 12.2 g of 7-oxo-2,3,4,5,6,7-hexahydrobenzothiazoline-2-one melting at 262° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03988444 |
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| Source dataset | uspto-grants-1976_10 |
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| ORD ID | ord-da88ff615b3442ddb69e294fc126dc05 |
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| Source note | uspto-grants-1976_10 |
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