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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 271635Generated: October 26, 2026

Allyl Alcohol → 3-(4-(Hydroxymethyl)phenyl)propanal

https://huagongshe.com/reaction/271635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl AlcoholHCID 7858—
ReactantEthyl AcetateHCID 8857—
Reactant4-Iodobenzyl alcoholHCID 29012—
ReactantSodium BicarbonateHCID 516892—
Catalystpalladium(II) acetateHCID 167845—
CatalystTetrabutylammonium chloride hydrateHCID 16212273—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product3-(4-(Hydroxymethyl)phenyl)propanalHCID 53425276—

Reaction Conditions

Temperature60 °C

Reaction Steps

10.5 mL (152.8 mmol) allylalcohol, 18.8 g (62.2 mmol) Tetrabutylammonium chloride monohydrate, 12.8 g (152.8 mmol) NaHCO3 and 0.75 g (3.1 mmol) Pd(OAc)2 is added to a solution of 15.0 g (62.2 mmol) 4-iodobenzylalcohol in 100 mL DMF at RT under an N2 atmosphere and the reaction solution is heated to 60° C. for 3 h. The solvent is eliminated i.vac., the residue combined with 250 mL EtOAc and 80 mL water and suction filtered through a fibreglass filter. 80 mL NaCl solution are added to the filtrate, the phases are separated and the organic phase is dried over MgSO4. After the desiccant and solvent have been eliminated the residue is purified by column chromatography on silica gel (gradient: cyc/EtOAc 3:1 after cyc/EtOAc 1:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07452911B2
Source datasetuspto-grants-2008_11
ORD IDord-c091aec98fb744dc835629a691d3c1bb
Source noteuspto-grants-2008_11