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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757506Generated: October 26, 2026

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

https://huagongshe.com/reaction/1757506

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-hydroxy-benzaldehyde (2.69 g, 22 mmol), triphenylphosphine (5.8 g, 22 mmol) and diethylazadicarboxylate (3.83 g, 22 mmol) in tetrahydrofuran (25 mL). Stirat 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 filtrat in vacuo. Purify by silica gel chromatography to give 3-(4-ethoxybenzyloxy)benzaldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05446068
Source datasetuspto-grants-1995_08
ORD IDord-baa273998de7493cab3c50249b31f3bf
Source noteuspto-grants-1995_08