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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25834Generated: October 26, 2026

Methanol → 3-Benzyloxybenzaldehyde

https://huagongshe.com/reaction/25834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant3-BenzylphenolHCID 140897—
SolventChloroformHCID 6212—
Product3-BenzyloxybenzaldehydeHCID 74342—

Reaction Steps

To a solution of 3-hydroxylbenzaldehyde 31 (5.0 g, 40 mmol) and K2CO3 (27.2 g, 197 mmol) in 200 ml CHCl3: 100 ml MeOH was added benzylbromide (5.9 ml, 49 mmol). The suspension was refluxed under nitrogen overnight. The solvent was removed by evaporation and the resulting oil was taken up in DCM and washed with water and brine and dried (Na2SO4). The crude product was purified by column chromatography to yield the product as a viscous oil which solidified upon sitting (8.48 g, 40 mmol, 98%). m.p. 46°. 1H NMR (500 MHz, CDCl3) δ 9.97 (s, 1H), 7.48-7.25 (m, 9H), 5.13 (s, 2H). 13C NMR (125 MHz, CD3OD) δ 191.8, 159.2, 137.8, 136.3, 130.0, 128.6, 128.1, 127.5, 123.41, 121.9, 113.3, 70.0. HRMS (EI) m/e calcd for C14H12O2: 212.08373, found: 212.0827.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06858600B2
Source datasetuspto-grants-2005_02
ORD IDord-56afacbd8edf4ddb94d3f3ca93a30eb6
Source noteuspto-grants-2005_02