HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
alpha-Chloro-o-xylene → 2-[(2-Methylbenzyl)thio]-cis-4,5-diphenyl-4,5-dihydro-1H-imidazole Hydrochloride
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | alpha-Chloro-o-xylene | HCID 11093 | — |
| Edukt | cis-4,5-Diphenylimidazolidine-2-thione | HCID 45258634 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 2-[(2-Methylbenzyl)thio]-cis-4,5-diphenyl-4,5-dihydro-1H-imidazole Hydrochloride | HCID 68567166 | 56% |
Reaktionsschritte
A mixture of intermediate 25 (200 mg, 0.786 mmol) and 2-methylbenzyl chloride (0.204 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 174 mg of the product 227. 1H NMR (DMSO-d6) δ 11.28 (s, 2 H), 7.68 (m, 1 H), 7.55-7.20 (m, 3 H), 7.20-7.00 (m, 6 H), 7.00-6.90 (m, 4 H), 5.82 (s, 2 H), 4.81 (s, 2 H), 2.44 (s, 3 H); MS: m/z 359 (M++1).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07741493B2 |
| Quelldatensatz | uspto-grants-2010_06 |
| ORD ID | ord-72cd2c4e099f47c8b31ac4d7f85f95f4 |
| Quellennotiz | uspto-grants-2010_06 |