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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 640233Generated: October 29, 2026

3-Hydroxybenzaldehyde → 3-Benzyloxybenzaldehyde

https://huagongshe.com/reaction/640233

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxybenzaldehydeHCID 101—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
SolventDimethylformamideHCID 6228—
Product3-BenzyloxybenzaldehydeHCID 7434299%

Reaction Steps

3-Hydroxybenzaldehyde (3 g, 24.6 mmol) and potassium carbonate (10.2 g, 73.8 mmol) were suspended in N,N-dimethylformamide (60 mL). Benzyl bromide (3.21 mL, 27.1 mmol) was added to this suspension, and stirred for 14 hours at room temperature. This mixture was partitioned into ethyl acetate and water. The organic layer was separated, washed with water, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure, and the residue was purified by silica gel column chromatography (heptane:ethyl acetate=4:1-1:1) to obtain the title compound (5.16 g, 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07691882B2
Source datasetuspto-grants-2010_04
ORD IDord-e646ac53dfb24b5ca920fa50db0aa5a8
Source noteuspto-grants-2010_04