HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron tribromide → 1-(4-Hydroxybenzyl)imidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | N-p-methoxybenzylimidazole | HCID 578587 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(4-Hydroxybenzyl)imidazole | HCID 193822 | 91% |
Reaction Steps
To a stirred solution of the compound of Step A (16.3 g, 86.1 mmole) in methylene chloride (860 ml) cooled to 5° C., was added boron tribromide (32.6 ml, 344.4 mmole) dropwise over 15 minutes. After 2 hours at 5° C., the reaction was quenched with methanol dropwise, evaporated to dryness, and redissolved in methanol, water, and methylene chloride The pH was adjusted to 8.4 with sodium hydroxide. The organic layer was dried over sodium sulfate and evaporated to dryness to give N-p-hydroxybenzylimidazole (13.6 g, 91%) which was used without further purification:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06472387B1 |
| Source dataset | uspto-grants-2002_10 |
| ORD ID | ord-58c6b5c69ae54f289938ab869caad5c5 |
| Source note | uspto-grants-2002_10 |