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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6494Generated: October 25, 2026

3-Hydroxybenzaldehyde → 3-(4-Ethoxybenzyloxy)benzaldehyde

https://huagongshe.com/reaction/6494

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxybenzaldehydeHCID 101—
ReactantTriphenylphosphineHCID 11776—
Reactant4-Ethoxybenzyl alcoholHCID 80345—
SolventTetrahydrofuranHCID 8028—
Product3-(4-Ethoxybenzyloxy)benzaldehydeHCID 19388223—

Reaction Steps

Mix 4-ethoxybenzyl alcohol (3.35 g. 22 mmol), 3-hydroxybenzaldehyde (2.69 g, 22 mmol), triphenylphosphine (5.8 g, 22 mmol) and diethylazadicarboxylate (3.83 g, 22 mmol) in tetrahydrofuran (25 mL). Stir at room temperature under anhydrous atmosphere until the reaction is done. Concentrate the solution in vacuo and dilute with a small quantity of ethyl ether. Filter any precipitate and concentrate the filtrate in vacuo. Purify by silica gel chromatography to give 3-(4-ethoxybenzyloxy)benzaldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05248825
Source datasetuspto-grants-1993_09
ORD IDord-43a0aaa7336a47c9a189d7a4c5585e94
Source noteuspto-grants-1993_09