HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2,3-Dimethylphenyl)(1-trityl-1H-imidazol-5-yl)methanone → 1-(2,3-Dimethylphenyl)-2-phenyl-1-(1-trityl-1h-imidazol-5-yl)ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2,3-Dimethylphenyl)(1-trityl-1H-imidazol-5-yl)methanone | HCID 42631463 | — |
| Reactant | HCID 178419663 | HCID 178419663 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(2,3-Dimethylphenyl)-2-phenyl-1-(1-trityl-1h-imidazol-5-yl)ethanol | HCID 57437678 | — |
Reaction Steps
A solution of (2,3-dimethylphenyl)(l-trityl-1H imidazol-5-yl)methanone (450 mg, 1.01 mmol) in dichloromethane (25 mL) at room temperature was treated with benzyl magnesium bromide (1.51 mmol) and allowed to react at room temperature and the reaction mixture was then stirred at room temperature for 5 hours. The mixture was quenched with water (10 mL) and a sat. solution of ammonium chloride (10 mL). The residue was isolated in a typical aqueous to give 1-(2,3-dimethylphenyl)-2-phenyl-1-(1-trityl-1H-imidazol-5-yl)ethanol (Intermediate 8) crude, which was taken to the next step without any purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07902247B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-c655188af47c4cffae7479f12d8bed46 |
| Source note | uspto-grants-2011_03 |