Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504583Generated: October 30, 2026

3-Hydroxybenzaldehyde → 3-Benzyloxybenzaldehyde

https://huagongshe.com/reaction/1504583

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxybenzaldehydeHCID 101—
ReactantDichloromethaneHCID 6344—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product3-BenzyloxybenzaldehydeHCID 74342103.9%

Reaction Steps

In acetonitrile (50 mL) solvent, benzyl bromide (4.6 mL, 38.68 mmol) was added to a solution including 3-hydroxybenzaldehyde (5.0 g, 40.94 mmol) and potassium carbonate (8.49 g, 61.43 mmol), and the reaction mixture was refluxed for 3 hours. After cooling, the reaction mixture was distributed between methylene chloride and water. An organic layer was dried by using MgSO4 and filtered. The filtrate was evaporated, and water was added to the resultant solid. The solid was filtered and washed with water to obtain Compound 123a (8.53 g, 98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216148B2
Source datasetuspto-grants-2015_12
ORD IDord-bb6eaa84b169440ea6f4eca46c35b8dc
Source noteuspto-grants-2015_12