HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Sulfide → 2-(3,4-Dichlorophenyl)ethanethioamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Sulfide | HCID 402 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (3,4-Dichlorophenyl)acetonitrile | HCID 76690 | — |
| Reactant | Thioacetamide | HCID 2723949 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(3,4-Dichlorophenyl)ethanethioamide | HCID 21504264 | 55% |
Reaction Steps
Hydrogen sulfide (gas) was bubbled into a solution of (3,4-dichloro-phenyl)-acetonitrile (1.86 g, 10 mmol, 1.0 eq)) and triethyl amine (10 mmol, 1 eq) in ethanol (10 ml) for about 1 hour. After 1 hour the reaction mixture capped and stirred at room temperature overnight. TLC showed that most of nitrile was converted to thioacteamide. Excess of H2S was removed by bubbling nitrogen into the reaction mixture for 30 min. The reaction mixture was then concentrated and purified by silica gel chromatography (ISCO system, 30-60% ethylacetate/hexane) to give the title compound (1213) (55% yield)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08017629B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-3682921ec6d84266a9d48eaf4f9b19fc |
| Source note | uspto-grants-2011_09 |