HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Sulfide → 1,5-Dimethyl-1H-pyrrole-2-carbothioamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Sulfide | HCID 402 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,5-Dimethylpyrrole-2-carbonitrile | HCID 91812 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1,5-Dimethyl-1H-pyrrole-2-carbothioamide | HCID 15076237 | — |
Reaction Steps
5 g of 2cyano-1,5-dimethylpyrrol are dissolved in 40 ml of ethanol and treated with 10 ml of triethylamine. 50 ml of an ethanolic H2S solution (3.8 g/100 ml) are added and the mixture is heated for ca. 15 hours in an autoclave at 70°. The reaction mixture is cooled and the solvent is evaporated off to obtain ca. a quarter of its volume. 1,5-dimethylpyrrol-2-carbothioamide crystallizes upon cooling at 0° in the form of a light yellow precipitate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07317101B2 |
| Source dataset | uspto-grants-2008_01 |
| ORD ID | ord-d18276a010bb40719a9bd807eca3fa06 |
| Source note | uspto-grants-2008_01 |