Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 597525 | HCID 597525 | — |
| Reactant | 1-Benzyl-1H-imidazole-5-carboxaldehyde | HCID 2773239 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | HCID 178479004 | HCID 178479004 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 19904266 | HCID 19904266 | — |
Reaction Steps
The Gringnard reagent, diphenylethanyl magnesium chloride, is prepared by the usual way from diphenylethanylchloride (0.01 mol) and magnesium turnings (0.01 mol) in dry diethylether (30 ml). 1-benzyl-5-imidazole aldehyde (0.005 mol) is dissolved in dry diethylether and the Grignard reagent is added dropwise to the solution. The reaction mixture is refluxed for 3 hours. The reaction is then poured into 2N hydrochloric acid and extracted with diethylether. The water phase is made basic with sodium hydroxide and then extracted with ethyl acetate. The ethyl acetate phase is dried and evaporated. The residue is purified by flash-chromatography eluating with methylene chloride-methanol mixture (9.5:0.5). M.p. of the product as base is 188°-190° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05098923 |
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| Source dataset | uspto-grants-1992_03 |
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| ORD ID | ord-d4998a79709845d5b44fcc6ba5b828bb |
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| Source note | uspto-grants-1992_03 |
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