HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-Phenyl-1-(2,4,6-trimethylbenzoyl)-1H-imidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Triethylamine hydrochloride | HCID 11130 | — |
| Reactant | 2-Phenylimidazole | HCID 69591 | — |
| Reactant | 2,4,6-Trimethylbenzoyl chloride | HCID 97038 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Phenyl-1-(2,4,6-trimethylbenzoyl)-1H-imidazole | HCID 3023044 | 78.3% |
Reaction Steps
144.2 g (1.00 mole) of 2-phenylimidazole are dissolved at 90° C. in 900 ml of toluene. 104.2 g (1.03 moles) of triethylamine are added to this solution, and a solution of 182.6 g (1.00 mole) of 2,4,6-trimethylbenzoyl chloride in 300 ml of toluene is added dropwise at 90° C. in the course of 2 hours, triethylamine hydrochloride being precipitated. The latter is filtered off with suction at room temperature and extracted by washing with toluene. Concentrating the filtrate gives 296 g of crude product, recrystallisation of which from 580 ml of acetonitrile gives a total of 227.3 g of 1-(2,4,6-trimethylbenzoyl)-2-phenylimidazole (78.3% of theory).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04579916 |
| Source dataset | uspto-grants-1986_04 |
| ORD ID | ord-055f068c72994a5784778f01c32dd378 |
| Source note | uspto-grants-1986_04 |