HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1834888Generated: October 26, 2026
Potassium Hydroxide → 2-[O-(N-Dimethylaminosulfenyl-N-methylcarbamoyl)oximino]-3,3-dimethyltetrahydro-1,4-thiazin-5-one
https://huagongshe.com/reaction/1834888
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | N-methyl-N-(dimethylaminosulfenyl)carbamoyl fluoride | HCID 12799216 | — |
| Reactant | 6-(Hydroxyimino)-5,5-dimethylthiomorpholin-3-one | HCID 71386949 | — |
| Catalyst | Dicyclohexano-18-crown-6 | HCID 85955 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-[O-(N-Dimethylaminosulfenyl-N-methylcarbamoyl)oximino]-3,3-dimethyltetrahydro-1,4-thiazin-5-one | HCID 54253931 | 68.6% |
Reaction Steps
A mixture of 5.8 g of 2-oximino-3,3-dimethyltetrahydro-1,4-thiazin-5-one, 200 ml dioxane, 2.1 g powdered potassium hydroxide and 0.1 g dicyclohexyl-18-crown-6, was charged to a stirred flask and 5.3 g of N-methyl-N-(dimethylaminosulfenyl)carbamoyl fluoride was added at 30° C over a 1-minute period. The reaction mixture was stirred overnight at room temperature and then added to cold water and stirred for 5 minutes. The resulting mixture was extracted with methylene chloride. The methylene chloride layer was washed thoroughly with water and then dried with magnesium sulfate. The methylene chloride was stripped from the product under reduced pressure and the crystalline residue was recrystallized from ethylene acetate to provide 7.0 g of 2-[O-(N-Dimethylaminosulfenyl-N-methylcarbamoyl)oximino]-3,3-dimethyltetrahydro-1,4-thiazin-5-one, m.p. 165°-167° C. An nmr spectrum supported the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04071627 |
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| Source dataset | uspto-grants-1978_01 |
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| ORD ID | ord-ac3c7f305bd2427b899bfa08c8539b4d |
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| Source note | uspto-grants-1978_01 |
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