HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 543320Generated: October 31, 2026
Imidazole → [3-(1H-Imidazol-1-yl)phenyl](2,4,6-trimethylphenyl)methanone
https://huagongshe.com/reaction/543320
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 13457470 | HCID 13457470 | — |
| Solvent | Hexamethylphosphoramide | HCID 12679 | — |
| Product | [3-(1H-Imidazol-1-yl)phenyl](2,4,6-trimethylphenyl)methanone | HCID 13247704 | 80.4% |
Reaction Steps
To a suspension of 2.9 g of sodium hydride (60% dispersion in mineral oil) in 50 ml of hexamethylphosphoric triamide is added 5.3 g of imidazole over a 30 minute period under heating at 40° C. After the addition is complete, the mixture is stirred at room temperature for an hour. To the reaction mixture is added 16.6 g of 3-fluoro-2',4',6'-trimethylbenzophenone and the mixture is stirred at 70° C. for 24 hours. The reaction solution is poured into ice-cold water and extracted with ethyl acetate. The ethyl acetate layer is washed with water, dried and concentrated. The residue is recrystallized from a mixture of toluene and isopropyl ether to give 16 g of 3-(1-imidazolyl)-2',4',6'-trimethylbenzophenone as white crystals, melting at 134°-136° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04661603 |
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| Source dataset | uspto-grants-1987_04 |
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| ORD ID | ord-70fc6b9c68a44a549739d55c9572de17 |
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| Source note | uspto-grants-1987_04 |
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