HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → {[(2-Methyl-1-nitropropan-2-yl)sulfanyl]methyl}benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | Benzyl mercaptan | HCID 7509 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Water | HCID 962 | — |
| Product | {[(2-Methyl-1-nitropropan-2-yl)sulfanyl]methyl}benzene | HCID 14613816 | — |
Reaction Steps
Acetone (25 g), benzyl mercaptan (53 g), nitromethane (26.2 g), and piperidine (8 cm3) were dissolved in benzene (150 cm3) and the mixture heated under reflux with azeotropic removal of water. After 48 h the reaction mixture was allowed to cool and washed first with dilute hydrochloric acid, then with water. The remaining solution was dried (MgSO4) and the solvent then removed under reduced pressure to give the nitro system (76.5 g, 85%). This material was sufficiently pure to be used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05312904 |
| Source dataset | uspto-grants-1994_05 |
| ORD ID | ord-f1507ad9f5b4440ba0987a3e0f60a33b |
| Source note | uspto-grants-1994_05 |