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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916532Generated: October 26, 2026

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

https://huagongshe.com/reaction/1916532

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 numberUS08618132B2
Source datasetuspto-grants-2013_12
ORD IDord-041ad69736544f918c4e009bc3042ac1
Source noteuspto-grants-2013_12