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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757509Generated: October 26, 2026

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

https://huagongshe.com/reaction/1757509

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 (25mL). Stir at room temperature under anhydrous atmosphere until the reactionis done. Concentrate the solution in vacuo and dilute with a small quantityof 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 numberUS05446068
Source datasetuspto-grants-1995_08
ORD IDord-819adadf5e1844e09c815c34be2bed7e
Source noteuspto-grants-1995_08