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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1,1,1-Trichloro-2-nitroethane | HCID 10954103 | — |
| Reactant | 1-Methylamino-3-propanethiol | HCID 12634510 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Tetrahydro-3-methyl-2-(nitromethylene)-1,3-thiazine | HCID 54288034 | 95.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04625025 |
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| Source dataset | uspto-grants-1986_11 |
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| ORD ID | ord-4e1b2f18eefa4de99bf11981f64facae |
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| Source note | uspto-grants-1986_11 |
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