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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1891667Generated: November 2, 2026

3-Hydroxybenzaldehyde → 3-Benzyloxybenzaldehyde

https://huagongshe.com/reaction/1891667

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 numberUS08507530B2
Source datasetuspto-grants-2013_08
ORD IDord-4cbedc773cb7492dbe47745d462b6eba
Source noteuspto-grants-2013_08