HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → N-[2-(1-cyclohexenyl)ethyl]-N'-(2-benzimidazolyl)thiourea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2-(1-Cyclohexenyl)ethylamine | HCID 76938 | — |
| Reactant | N-(1H-benzo[d]imidazol-2-yl)-1H-imidazole-1-carbothioamide | HCID 19704123 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-[2-(1-cyclohexenyl)ethyl]-N'-(2-benzimidazolyl)thiourea | HCID 54139746 | 55% |
Reaction Steps
A solution of 1-[(2-benzimidazolyl)thiocarbamoyl]imidazole (1.22 g, 5.0 mmol) and 2-(1-cyclohexenyl)ethylamine (0.64 g, 5.0 mmol) in N,N-dimethylformamide (20 mL) was stirred at 90° C. for 2 h. The reaction was cooled to room temperature, poured into ethyl acetate, washed with water, 1N aqueous HCl, water, saturated sodium bicarbonate, and brine. The organic layer was concentrated and the resultant solid was crystallized from EtOAc to provide 0.82 g (55%) of the titled product as yellow needles:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05593993 |
| Source dataset | uspto-grants-1997_01 |
| ORD ID | ord-809668ea177944a893e1483a695e3f3c |
| Source note | uspto-grants-1997_01 |