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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732091Generated: October 30, 2026

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

https://huagongshe.com/reaction/1732091

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant1,1,1-Trichloro-2-nitroethaneHCID 10954103—
Reactant1-Methylamino-3-propanethiolHCID 12634510—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductTetrahydro-3-methyl-2-(nitromethylene)-1,3-thiazineHCID 5428803495.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

Into 40 ml of methanol were added 5.0 g of 1-methylamino-3-propanethiol and 1.0 g 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 2.2 g of caustic soda dissolved in 25 ml of methanol and a solution of 3.5 g of 2,2,2-trichloro-1-nitroethane 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. The reaction was exothermic and the liquid temperature was maintained at lower than 10° C. (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 3.27 g of tetrahydro-3-methyl-2-(nitromethylene)- 1,3-thiazine (yield: 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04625025
Source datasetuspto-grants-1986_11
ORD IDord-4e1b2f18eefa4de99bf11981f64facae
Source noteuspto-grants-1986_11