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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213565Generated: October 27, 2026

Benzyl Bromide → 4-[(4-Methoxyphenyl)methoxy]-3-(phenylmethoxy)benzaldehyde

https://huagongshe.com/reaction/2213565

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantCesium carbonateHCID 10796—
Reactant3-Hydroxy-4-[(4-methoxyphenyl)methoxy]benzaldehydeHCID 11230648—
SolventDimethylformamideHCID 6228—
Product4-[(4-Methoxyphenyl)methoxy]-3-(phenylmethoxy)benzaldehydeHCID 2195750871.4%

Reaction Steps

Benzyl bromide (13.56 mL, 0.11 mol, 1.1 eq) was added to a solution of 3-hydroxy-4-[(4-methoxyphenyl)methoxy]benzaldehyde (26.91 g, 0.10 mL, 1 eq) and cesium carbonate (20.37 g, 0.06 mol, 0.6 eq) in N,N-dimethylformamide (150 mL). The reaction mixture was stirred overnight and then concentrated in vacuo. The residual solution was diluted with ethyl acetate (200 mL) and washed with water (200 mL), saturated sodium chloride solution (3×200 mL), and 0.5M aqueous sodium hydroxide (3×200 mL), then dried over sodium sulfate and evaporated in vacuo. This gave a gummy solid which was recrystallized from ethyl acetate and petroleum ether to give the product as a pale brown powder (25.93 g, 71%). 1H NMR (CDCl3) δ 9.81 (s, 1H, O═C—H), 5.21 (s, 2H, CH2Ar), 5.20 (s, 2H, CH2Ar), 3.84 (s, 3H, OCH3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105554B2
Source datasetuspto-grants-2006_09
ORD IDord-8d89b83898284051b61678a6629c7fb6
Source noteuspto-grants-2006_09