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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 744800Generated: October 26, 2026

Sodium hydride → 4-(Benzyloxy)-3-(3-methoxypropoxy)benzaldehyde

https://huagongshe.com/reaction/744800

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant1-Bromo-3-methoxypropaneHCID 524551—
Reactant4-Benzyloxy-3-hydroxybenzaldehydeHCID 561369—
SolventDimethylformamideHCID 6228—
Product4-(Benzyloxy)-3-(3-methoxypropoxy)benzaldehydeHCID 21458608—

Reaction Steps

A solution of 28.8 g of 4-benzyloxy-3-hydroxy-benzaldehyde in 100 ml of dimethyl-formamide is added dropwise to a suspension of 5.54 g of NaH (60% dispersion in mineral oil) in 150 ml of absolute dimethylformamide. The reaction mixture is stirred at room temperature. After 30 minutes, a solution of 29 g of 3-methoxybromopropane in 120 ml of dimethylformamide is added thereto, and the mixture is stirred at room temperature for a further 4 hours and is then concentrated by evaporation under reduced pressure. The residue is partitioned between diethyl ether and water. The combined organic phases are dried over sodium sulfate and concentrated by evaporation, and the residue is purified by FC (100 g of silica gel, dichloromethane), yielding the title compound, which crystallises spontaneously: Rf (dichloromethane/diethyl ether)=0.44.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05559111
Source datasetuspto-grants-1996_09
ORD IDord-d93c33ccc6b4450a84c93e8ac0692345
Source noteuspto-grants-1996_09