HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Sulfide → (3-Methylphenyl)ethanethioamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Sulfide | HCID 402 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | m-Methylphenylacetonitrile | HCID 76279 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | (3-Methylphenyl)ethanethioamide | HCID 21504242 | — |
Reaction Steps
Hydrogen sulphide gas was passed through a solution of 3-methylphenylacetonitrile (26.2 g.) in dry pyridine (30 ml.) and triethylamine (20.2 g.) during 5 hours. The solution was allowed to stand at room temperature overnight and then evaporated under reduced pressure. The residue was dissolved in benzene and precipitated with light petroleum (b.p. 60°-80°). The product, m.p. 66°-69°, was recrystallised from a mixture of ethanol and water to give pure 3-methylphenyl(thioacetamide), m.p. 76°-78°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03987158 |
| Source dataset | uspto-grants-1976_10 |
| ORD ID | ord-dbb994dd55a34e92a3fa458032a07d4e |
| Source note | uspto-grants-1976_10 |