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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6497Generated: October 25, 2026

3-Hydroxybenzaldehyde → 3-(4-(Dimethylamino)-benzyloxy) benzaldehyde

https://huagongshe.com/reaction/6497

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxybenzaldehydeHCID 101—
ReactantTriphenylphosphineHCID 11776—
Reactant4-Dimethylaminobenzyl alcoholHCID 137166—
SolventTetrahydrofuranHCID 8028—
Product3-(4-(Dimethylamino)-benzyloxy) benzaldehydeHCID 39204907—

Reaction Steps

Mix 4-(dimethylamino)benzyl 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 filtrat in vacuo. Purify by silica gel chromatography to give 3-(4-(dimethylamino)-benzyloxy) benzaldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05248825
Source datasetuspto-grants-1993_09
ORD IDord-7100e9edbf604a50bcb345884fc1b480
Source noteuspto-grants-1993_09