HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 2-Hydroxy-5-nitrothiocarbanilide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 1,2-Diaminocyclohexane | HCID 4610 | — |
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Hydroxy-5-nitrothiocarbanilide | HCID 2823848 | — |
Reaction Steps
To a mixture of 67 g. of carbon disulfide in 300 ml. of ethanol is added dropwise with stirring a solution of 100 g. of 1,2-diaminocyclohexane in 100 ml. of ethanol. The resulting solution is stirred one-half hour after addition; liquid eliminated and the residue dissolved in 300 ml. of water and heated at reflux for 18 hours. The precipitate which forms on cooling is filtered off, washed with water and then with ether and dried under reduced pressure to obtain 3a,4,5,6,7,7a-hexahydro-2-benzimidazolin-thione, m.p. 170°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03963720 |
| Source dataset | uspto-grants-1976_06 |
| ORD ID | ord-725f456e7c124d14b2d6b200aa96d63c |
| Source note | uspto-grants-1976_06 |