HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Phenylbenzyl chloride → 2-[(4-Phenylbenzyl)thio]-cis-4,5-diphenyl-4,5-dihydro-1H-imidazole Hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Phenylbenzyl chloride | HCID 15463 | — |
| Reactant | cis-4,5-Diphenylimidazolidine-2-thione | HCID 45258634 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-[(4-Phenylbenzyl)thio]-cis-4,5-diphenyl-4,5-dihydro-1H-imidazole Hydrochloride | HCID 68569646 | 57.1% |
Reaction Steps
A mixture of intermediate 25 (200 mg, 0.786 mmol) and 4-phenylbenzyl chloride (0.318 mg, 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 205 mg of the product 207. 1H NMR (DMSO-d6) δ 11.24 (s, 2H), 7.90-7.60 (m, 6H), 7.60-7.30 (m, 3H), 7.20-6.90 (m, 6H), 6.90-6.65 (m, 4H), 5.79 (s, 2H), 4.85 (s, 2H); MS: m/z 421 (M++1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07326792B2 |
| Source dataset | uspto-grants-2008_02 |
| ORD ID | ord-0e32d46e892b4d52a1a9dfa1b5aa651d |
| Source note | uspto-grants-2008_02 |