HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzenesulfenyl chloride → 1-Methyl-2-[nitro(phenylsulfanyl)methylidene]imidazolidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzenesulfenyl chloride | HCID 11008040 | — |
| Reactant | 1-Methyl-2-(nitromethylidene)imidazolidine | HCID 70250046 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 1-Methyl-2-[nitro(phenylsulfanyl)methylidene]imidazolidine | HCID 70639009 | — |
Reaction Steps
14.6 g of phenylsulfenyl chloride was added dropwise to a cooled, stirred solution of 14.3 g of Compound 1 in 250 ml of pyridine. The mixture was allowed to stand overnight at room temperature, then excess pyridine was recovered on a rotary evaporator. The residue was treated with 250 ml of water and the mixture extracted with methylene chloride. The combined extracts were dried and the solvent evaporated to give a crystalline solid which was triturated with ethyl acetate, then ethanol, to yield 25, as a yellow solid, melting point: 170° - 173°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03969354 |
| Source dataset | uspto-grants-1976_07 |
| ORD ID | ord-55756baa408e4d72b2cff268dee583fb |
| Source note | uspto-grants-1976_07 |