Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Sulfide | HCID 402 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (1-Methyl-1H-imidazol-2-yl)acetonitrile | HCID 817716 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 20138267 | HCID 20138267 | — |
Reaction Steps
Hydrogen sulfide was bubbled to a solution of 1.4 gm (11.5 mmole) of N-methyl-2-cyanomethylimidazole and 10 ml dry pyridine stirred in a medium pressure glass Carius tube at 0° C. Then 1.5 equivalents of triethylamine was added (2.50 ml) and the pressure tube was sealed and heated on a steam bath for 4 hours. It was cooled and cracked open to vent any excess hydrogen sulfide. The product crystallized out of the solution when it was cooled to 0° C. The crystals were filtered and washed with 2×5 ml of hexane to afford 1.29 gm of N-methyl-2-thioacetamidioimidazole, m.p. 155°-160° C. (decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04746669 |
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| Source dataset | uspto-grants-1988_05 |
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| ORD ID | ord-c4a807da85854d3895181b7918e89ce5 |
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| Source note | uspto-grants-1988_05 |
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