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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1157844Generated: November 4, 2026

Terephthalaldehyde → 4-(Hydroxymethyl)benzaldehyde

https://huagongshe.com/reaction/1157844

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 numberUS07807694B2
Source datasetuspto-grants-2010_10
ORD IDord-b52345b28b1741578d8e52995681ae45
Source noteuspto-grants-2010_10