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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280231Generated: November 1, 2026

Terephthalaldehyde → 4-(Hydroxymethyl)benzaldehyde

https://huagongshe.com/reaction/1280231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTerephthalaldehydeHCID 12173—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
Product4-(Hydroxymethyl)benzaldehydeHCID 55633051%

Reaction Steps

First, 2.06 g of terephthalaldehyde and 20 ml of ethanol were placed in a reaction vessel, to which 0.15 g of sodium borohydride was slowly added with stirring under ice cooling. After stirring at room temperature for 12 hours, the ethanol was evaporated. The residue was poured into diluted hydrochloric acid, and extracted with ethyl acetate. The ethyl acetate layer was washed twice with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 1.06 g (yield, 51%) of p-(hydroxymethyl)benzaldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06448444B1
Source datasetuspto-grants-2002_09
ORD IDord-3e312da4c4974e4884c6d02dce0b9a0d
Source noteuspto-grants-2002_09