HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chlorobenzyl chloride → 2-[(2-Chlorobenzyl)thio]-cis-4,5-diphenyl-4,5-dihydro-1H-imidazole Hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chlorobenzyl chloride | HCID 11906 | — |
| Reactant | cis-4,5-Diphenylimidazolidine-2-thione | HCID 45258634 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-[(2-Chlorobenzyl)thio]-cis-4,5-diphenyl-4,5-dihydro-1H-imidazole Hydrochloride | HCID 68571150 | 32.2% |
Reaction Steps
A mixture of intermediate 25 (200 mg, 0.786 mmol) and 2-chlorobenzyl chloride (0.198 mL, 1.57 mmol) in abs. EtOH (2 mL) is heated at 95° C. for 24 h. The reaction mixture is cooled to RT, evaporated to dryness, and the residue suspended in Et2O. The insoluble material is filtered to give 105 mg of the product 208. 1H NMR (DMSO-d6) δ 11.38 (s, 2H), 7.90-7.70 (m, 1H), 7.70-7.55 (m, 1H), 7.55-7.35 (m, 2H), 7.20-7.00 (m, 6H), 7.00-6.85 (m, 4H), 5.81 (s, 2H), 4.88 (s, 2H); MS: m/z 379 (M++1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07326792B2 |
| Source dataset | uspto-grants-2008_02 |
| ORD ID | ord-cd8cb0c569904338a899277dd47a801b |
| Source note | uspto-grants-2008_02 |