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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230122Generated: October 25, 2026

4-(Diethoxymethyl)benzaldehyde → 4-(Hydroxymethyl)benzaldehyde

https://huagongshe.com/reaction/230122

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Diethoxymethyl)benzaldehydeHCID 595993—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product4-(Hydroxymethyl)benzaldehydeHCID 55633089.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cold (0° C.) solution of 4-(diethyoxymethyl)benzaldehyde (5.2 g, 24 mmol) in MeOH (50 mL) was added NaBH4 (0.93 g, 24 mmol), and the reaction mixture was stirred for 3 hours. The MeOH was removed and the residue was taken up in DCM and diluted with water. The aqueous layer was extracted with DCM (3×50 mL). The combine organic layers were dried, filtered and concentrated. The crude oil was dissolved in MeOH (50 mL) and cooled to 0° C. To this was added 2N HCl (10.0 mL) in ether. The reaction mixture was left at room temperature for 24 hours. The MeOH was removed and the crude product was purified by flash column chromatography, eluting with EtOAc/Hexane (3:7) to yield 2.92 g of 4-(hydroxymethyl)benzaldehyde (11) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07566716B2
Source datasetuspto-grants-2009_07
ORD IDord-ee732d22252346e6b92541f5244d0cef
Source noteuspto-grants-2009_07