HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 1-benzyl-5-(1-hydroxy-4,4-diphenylbutyl)-1H-imidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,1'-(3-Bromopropylidene)bisbenzene | HCID 88333 | — |
| Reactant | 1-Benzyl-1H-imidazole-5-carboxaldehyde | HCID 2773239 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-benzyl-5-(1-hydroxy-4,4-diphenylbutyl)-1H-imidazole | HCID 14822290 | — |
Reaction Steps
Magnesium turnings (0.5 g) were covered with dry tetrahydrofuran (4 ml). 1-Bromo-3,3-diphenylpropane (5.6 g) in 20 ml of dry tetrahydrofuran was added dropwise. The mixture was stirred at reflux for one hour. After being cooled to room temperature, 3-benzyl-3H-imidazole-4-carbaldehyde (3.8 g) in 20 ml of dry tetrahydrofuran was added dropwise to the Grignard reagent and the mixture was refluxed for two hours. The cooled reaction mixture was poured into a cold diluted hydrochloric acid solution. Work-up of the mixture gave the crude product, which was converted to its hydrochloride salt in ethyl acetate using dry hydrochloric acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06388090B2 |
| Source dataset | uspto-grants-2002_05 |
| ORD ID | ord-1c2aeb91747747ec9fcb52c39d5ff6e5 |
| Source note | uspto-grants-2002_05 |