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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant1,4-DioxaneHCID 31275—
ReactantN-methyl-N-(dimethylaminosulfenyl)carbamoyl fluorideHCID 12799216—
Reactant6-(Hydroxyimino)-5,5-dimethylthiomorpholin-3-oneHCID 71386949—
CatalystDicyclohexano-18-crown-6HCID 85955—
SolventWaterHCID 962—
Product2-[O-(N-Dimethylaminosulfenyl-N-methylcarbamoyl)oximino]-3,3-dimethyltetrahydro-1,4-thiazin-5-oneHCID 5425393168.6%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04071627
Source datasetuspto-grants-1978_01
ORD IDord-ac3c7f305bd2427b899bfa08c8539b4d
Source noteuspto-grants-1978_01