HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Sulfide → 1-Acetyl-2,3-dihydro-1H-indole-2-carbothioamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Sulfide | HCID 402 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Acetyl-2,3-dihydro-1H-indole-2-carbonitrile | HCID 14819314 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 1-Acetyl-2,3-dihydro-1H-indole-2-carbothioamide | HCID 21914112 | — |
Reaction Steps
A solution of 1-acetyl-2,3-dihydro-1H-indole-2-carbonitrile (0.00988 mol) and Triethylamine (0.0197 mol) in pyridine (50 ml) was treated with hydrogen sulfide (gas) at room temperature via a bubbler for 2 hours and the resultant saturated reaction mixture was closed and allowed to set for 16 hours. The reaction mixture was poured into 200 ml of an ice water slurry. A voluminous precipitate formed. The mixture was recooled in an ice bath and the precipitate was collected by suction filtration, washed with cold water, and air dried, yielding 1.62 g of 1-acetyl-2,3-dihydro-1H-indole-2-carbothioamide (intermediate 13, mp. 194-195° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07947713B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-51e06ed143f74b3199050316cc7c01ec |
| Source note | uspto-grants-2011_05 |