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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1369941Generated: October 29, 2026

Boron tribromide → 1-(4-Hydroxybenzyl)imidazole

https://huagongshe.com/reaction/1369941

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantN-p-methoxybenzylimidazoleHCID 578587—
SolventDichloromethaneHCID 6344—
Product1-(4-Hydroxybenzyl)imidazoleHCID 19382291%

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 lever 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06579871B2
Source datasetuspto-grants-2003_06
ORD IDord-1a8e9a24fb3e4c5084a6db5cd5df6c68
Source noteuspto-grants-2003_06