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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 978605Generated: October 30, 2026

Hydrochloric Acid → Tetrahydro-3-methyl-2-(nitromethylene)-1,3-thiazine

https://huagongshe.com/reaction/978605

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant1,1-Dichloro-2-nitroetheneHCID 12219571—
Reactant1-Methylamino-3-propanethiolHCID 12634510—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductTetrahydro-3-methyl-2-(nitromethylene)-1,3-thiazineHCID 5428803498.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

Into 40 ml of methanol were added 5.0 g of 1-methylamino-3-propanethiol and 0.8 g of caustic soda, followed by stirring, to be completely dissolved therein. Then, the mixture was cooled to 0° C. While stirring the solution, a solution of 1.6 g of caustic soda dissolved in 25 ml of methanol and a solution of 2.8 g of 2,2-dichloronitroethylene diluted in 20 ml of methanol were added at the same time dropwise slowly over 50 minutes, and the reaction was carried out for one hour at about 8° C. After the reaction, the reaction mixture was neutralized to pH 7 with 3 N aqueous hydrochloric acid, and then with addition of 60 ml of water, extraction with 50 ml of methylene chloride was repeated four times. The extracts were concentrated to give 3.38 g of tetrahydro-3-methyl-2-(nitromethylene)-1,3-thiazine (yield: 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04665172
Source datasetuspto-grants-1987_05
ORD IDord-b92e1cb9685a4fa5a23cdd426fca6e64
Source noteuspto-grants-1987_05