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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1624225Generated: November 2, 2026

Terephthalaldehyde → 4-(Hydroxymethyl)benzaldehyde

https://huagongshe.com/reaction/1624225

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) δ 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 numberUS08778967B2
Source datasetuspto-grants-2014_07
ORD IDord-72f9fca1808043e7b4a98ff38e3cffb2
Source noteuspto-grants-2014_07