HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methylimidazole → (1-Methyl-1H-imidazol-2-yl)(phenyl)methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methylimidazole | HCID 1390 | — |
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (1-Methyl-1H-imidazol-2-yl)(phenyl)methanone | HCID 12325240 | 92.4% |
Reaction Steps
To a solution of N-methylimidazole (10.0 g, 122 mmol) in acetonitrile (120 mL) was added benzoyl chloride (14.1 mL, 122 mmol) followed by triethylamine (17.0 mL, 122 mmol), while keeping the internal temperature at 5° C. The mixture was stirred 18 h at room temperature. After filtration, the filtrate was concentrated in vacuo, diluted with ethyl acetate (200 mL) and sequentially washed with sat. aq. sodium bicarbonate (150 mL), water (100 mL) and brine (100 mL). The organic layer was dried over MgSO4 and concentrated in vacuo.to afford (1-methyl-1H-imidazol-2-yl)(phenyl)methanone [21.0 g, yield 83%; HPLC/MS: m/z=187 (M+H); log P(HCOOH)=1.38].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08981111B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-0c927385c33e4ab4a660860ae4ff4a8a |
| Source note | uspto-grants-2015_03 |