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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916578Generated: November 4, 2026

Allyl Alcohol → 3-(4-Bromophenyl)propanal

https://huagongshe.com/reaction/1916578

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl AlcoholHCID 7858—
Reactant1-Bromo-4-iodobenzeneHCID 11522—
ReactantSodium BicarbonateHCID 516892—
CatalystTetrabutylammonium ChlorideHCID 70681—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product3-(4-Bromophenyl)propanalHCID 11481288—

Reaction Conditions

Temperature60 °C

Reaction Steps

210 mg (0.86 mmol) Pd(OAc)2, 5.23 g (17.32 mmol) tetra-n-butylammonium chloride and 3.6 g NaHCO3 are added to a solution of 5.0 g (17.32 mmol) 4-bromo-iodo-benzene and 3.0 mL (43.67 mmol) allylalcohol in 30 mL DMF. The reaction solution is stirred for 2 h at 60° C. and diluted with 50 mL water. The aqueous phase is extracted with 50 mL EtOAc and the combined organic extracts are washed with 50 mL saturated NaCl solution. The organic phase is dried over Na2SO4 and the solvent is eliminated i.vac. Further purification is carried out by column chromatography on silica gel (cyc/EtOAc 3:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618132B2
Source datasetuspto-grants-2013_12
ORD IDord-e1b1308489f745358b8920534d10b34c
Source noteuspto-grants-2013_12