HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → (1H-Imidazol-1-yl)(2,4,6-trimethylphenyl)methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | 2,4,6-Trimethylbenzoyl chloride | HCID 97038 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (1H-Imidazol-1-yl)(2,4,6-trimethylphenyl)methanone | HCID 12852198 | 68% |
Reaction Steps
136 g (2.0 moles) of imidazole in 1,000 ml of ether are initially taken, and 146 g (0.8 mole) of 2,4,6-trimethylbenzoyl chloride are added dropwise to the stirred mixture in the course of 30 minutes at from 10° to 20° C. Stirring is continued for 5 hours at room temperature, and the precipitated imidazole hydrochloride is filtered off under suction, the filtrate is evaporated down and the residue is distilled to give 116.4 g (68% of theory) of N-(2,4,6-trimethylbenzoyl)-imidazole of boiling point 128° C./0.01 mbar.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04559398 |
| Source dataset | uspto-grants-1985_12 |
| ORD ID | ord-cb6db476f1d64cf1bb74236ed09f6f3a |
| Source note | uspto-grants-1985_12 |