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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298205Generated: October 29, 2026

Allyl Alcohol → 3-(3-Chlorophenyl)propionaldehyde

https://huagongshe.com/reaction/2298205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl AlcoholHCID 7858—
Reactant1-Chloro-3-iodobenzeneHCID 12269—
ReactantSodium BicarbonateHCID 516892—
CatalystTetrabutylammonium ChlorideHCID 70681—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product3-(3-Chlorophenyl)propionaldehydeHCID 1041957974%

Reaction Steps

A solution of 1-chloro-3-iodobenzene (9.63 g, 40.38 mmol), allyl alcohol (5.86 g, 100.96 mmol), sodium bicarbonate (8.48 g, 100.96 mmol), tetrabutylammonium chloride (11.22 g, 40.38 mmol), and Pd(OAc)2 (317 mg, 1.413 mmol) in 25 mL DMF was stirred at 50° C. for 18 h. The mixture was cooled to room temperature, diluted with water, and the aqueous solution was washed with EtOAc. The organic solution was washed with water followed by brine, dried over MgSO4, filtered and concentrated in vacuo. The product was purified via flash chromatography on silica gel (9:1 hexanes:EtOAc) to afford the title compound as an oil (5.04 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492412B2
Source datasetuspto-grants-2002_12
ORD IDord-4b06f7d67bdb4f60be1763997a8c7c63
Source noteuspto-grants-2002_12