HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → HCID 22258292, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | 5-Ethyl-2,4-dimethyl-1H-imidazole | HCID 15724086 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 22258292 | HCID 22258292 | — |
Reaction Steps
The compound is prepared as described in example X (step 4 and 5) with 1.00 g (8.05 mmol) 4-Ethyl-2,5-dimethyl-1H-imidazole (example XIII, step 1), 3.74 g (26.57 mmol) of benzoyl chloride and 2.85 g (28.18 mmol) of TEA in 20 ml acetonitrile. After reaction the solvent is evaporated under vacuum. The residue is extracted with toluene/water and the water phase is filtrated over a silica-layer. The solvent is evaporated under vacuum. The crude intermediate is directly transformed into 2-(4-Ethyl-5-methyl-1H-imidazol-2-yl)-1-phenylethanone hydrochloride. After the reaction the solvent is evaporated under vacuum. The residue is extracted with ethyl acetate/water. The water phase is concentrated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06984646B2 |
| Source dataset | uspto-grants-2006_01 |
| ORD ID | ord-8e24d90ed3234f5f9f0c5c6110af8157 |
| Source note | uspto-grants-2006_01 |