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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1,1-Dichloro-2-nitroethene | HCID 12219571 | — |
| 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 | 98.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04665172 |
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| Source dataset | uspto-grants-1987_05 |
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| ORD ID | ord-b92e1cb9685a4fa5a23cdd426fca6e64 |
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| Source note | uspto-grants-1987_05 |
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