HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Sulfide → 4′-Methyl[1,1′-biphenyl]-2-carbothioamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Sulfide | HCID 402 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Cyano-4'-methylbiphenyl | HCID 145512 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4′-Methyl[1,1′-biphenyl]-2-carbothioamide | HCID 21711274 | — |
Reaction Steps
First, 2.00 g of 2-cyano-4′-methyl-1,1′-biphenyl was dissolved in a mixture of 15, ml of methanol and 4.18 g of triethylamine, and hydrogen sulfide gas was bubbled thereinto at room temperature to the point of saturation. After keeping at room temperature for 3 days, the solution was kept at 50° C. for 6 hours. The reaction mixture was concentrated under reduced pressure, and the residue was extracted with ethyl acetate containing 1% hydrochloric acid. The organic layer was concentrated to give 2.18 g of 2-thiocarbamoyl-4′-methyl-1,1′-biphenyl. Yield, 92%; m.p., 111-115° C.; m/z, 227
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06277998B1 |
| Source dataset | uspto-grants-2001_08 |
| ORD ID | ord-29b42941e61e46c3ba8d58d0ec03a7e4 |
| Source note | uspto-grants-2001_08 |