HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Thiazole, 4-(4-chlorophenyl)-5-methyl-2-phenyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Thiobenzamide | HCID 683563 | — |
| Reactant | 2-Bromo-1-(4-chlorophenyl)propan-1-one | HCID 3788219 | — |
| Solvent | Water | HCID 962 | — |
| Product | Thiazole, 4-(4-chlorophenyl)-5-methyl-2-phenyl- | HCID 8036414 | 68.2% |
Reaction Steps
A mixture of 2-bromo-4′-chloropropiophenone (45.0 g), thiobenzamide (24.7 g), sodium acetate (14.8 g) and ethanol (400 mL) was stirred with heating under reflux for 3 hrs. The reaction mixture was poured into water, and the mixture was extracted with ethyl acetate. The organic layer was washed with water, dried over anhydrous magnesium sulfate and concentrated to give 4-(4-chlorophenyl)-5-methyl-2-phenylthiazole (35.1 g, 68%) as crystals. Recrystallization from ethyl acetate-hexane gave colorless prism crystals. melting point: 90–91° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07183276B2 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-e8f752d4746b4f299475521265f288a2 |
| Source note | uspto-grants-2007_02 |