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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7179Generated: October 26, 2026

Terephthalaldehyde → 4-(Hydroxymethyl)benzaldehyde

https://huagongshe.com/reaction/7179

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTerephthalaldehydeHCID 12173—
Reactant2-PyridinemethanamineHCID 19509—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product4-(Hydroxymethyl)benzaldehydeHCID 55633078%

Reaction Steps

Terephthaldicarboxaldehyde (30.02 g, 224 mmol), methanol (200 mL), palladium on activated carbon, (10%, 3.02 g) and 2-(aminomethyl)pyridine (2.3 mL, 22 mol, 0.01 mol equiv) were combined in a hydrogenation vessel and the reaction mixture was shaken on a Parr hydrogenator for 2.5 hours at 40 psi of hydrogen. The mixture was filtered through celite, the cake washed with methanol and the solvent from the eluent removed in vacuo. Purification of the crude product by column chromatography on silica gel (EtOAc/Hexanes, 1:1) afforded the title compound (23.8 g, 78%) as a white solid. 1H NMR (CDCl3) □ 4.80 (s, 2H), 7.53 (d, 2H, J=9 Hz), 7.87 (d, 2H, J=9 Hz), 10.00 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07084155B2
Source datasetuspto-grants-2006_08
ORD IDord-6cf759bc757143e7bba62c72bc8bb078
Source noteuspto-grants-2006_08