HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trityl chloride → [1-(triphenylmethyl)-1H-imidazol-4-yl]methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trityl chloride | HCID 6456 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 178519868 | HCID 178519868 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | [1-(triphenylmethyl)-1H-imidazol-4-yl]methanol | HCID 382182 | 82.3% |
Reaction Steps
Diisopropylethylamine (14 mL, 80 mmol) was added dropwise to a suspension of 4-imidazole methanol (5.4 g, 40 mmol) in CH3CN (15 mL) at 0° C. A homogeneous yellow solution was formed. To this solution was added triphenylmethyl chloride (11.2 g, 40 mmol). The reaction mixture was stirred at room temperature for 2 h. The resultant white precipitate was filtered and washed successively with saturated NaHCO3 aqueous solution (2×20 mL) and water (2×20 mL), then dried in a vacuum oven (45° C.) for 12 h to afford a white solid 11.2 g (82%) which was used in next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06156746 |
| Source dataset | uspto-grants-2000_12 |
| ORD ID | ord-397216c9a0894548895890bc7da0dfe8 |
| Source note | uspto-grants-2000_12 |