HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenacyl bromide → HCID 178521438, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenacyl bromide | HCID 6259 | — |
| Reactant | 3-(1-Trityl-1H-imidazol-4-YL)propan-1-OL | HCID 10832840 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178521438 | HCID 178521438 | — |
Reaction Steps
5 mmol of 3-(1-triphenylmethyl-1H-imidazol-4-yl)propanol and 5 mmol of 2-bromo-1-phenylethanone are stirred for 72 hours in methylene chloride. The solvent is evaporated off under reduced pressure and the residue is refluxed for 1 hour in 30 ml of 2N HCl and 30 ml of acetone. The solvent is evaporated off under reduced pressure and triphenylmethanol is extracted using diethyl ether. The aqueous phase is alkalized with ammonia, and the crude product is extracted with diethyl ether, purified by rotatory chromatography and crystallized as hydrogen maleate from diethyl ether and ethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06248765B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-29924635e3794ff6b334726d05ba47e3 |
| Source note | uspto-grants-2001_06 |