HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → N-Methyl-1-(methylsulfanyl)-2-nitroethan-1-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | 1-Methylthio-1-methylamino-2-nitroethylene | HCID 123549 | — |
| Reactant | 5-[[(2-Aminoethyl)thio]methyl]-N-methyl-2-furanmethanamine | HCID 20209492 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-Methyl-1-(methylsulfanyl)-2-nitroethan-1-amine | HCID 15788612 | — |
Reaction Steps
A solution of 2-[[[5-(methylamino)methyl-2-furanyl]methyl]thio]ethanamine (10 g, 0.05 mole) and N-methyl-1-methylthio-2-nitroetheneamine (7.4 g) in water (25 ml) was stirred at 50° for 2 hr. Acetone (350 ml) was added and the solvent was removed by distillation at atmospheric pressure until 275 ml of distillate had been collected. Ethanolic hydrogen chloride (2M; 27.5 ml) was added to the residue and the solution was stirred overnight at room temperature. The product (11.0 g) m.p. 161°, was collected and recrystallised from ethanol as a colourless microcrystalline solid (10.1 g) m.p. 162°. Analysis Found: C, 42.6; H, 6.3; N, 16.4. C12H20N4O3S.HCl requires: C, 42.8; H, 6.2; N, 16.6%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04128658 |
| Source dataset | uspto-grants-1978_12 |
| ORD ID | ord-879e2c1022f9429e8dc3684aeda99831 |
| Source note | uspto-grants-1978_12 |