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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588863Generated: October 26, 2026

Allyl Alcohol → 3-(5-Bromo-4-chloro-2-methoxyphenyl)propanal

https://huagongshe.com/reaction/588863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl AlcoholHCID 7858—
ReactantSodium BicarbonateHCID 516892—
Reactant1-Bromo-2-chloro-5-iodo-4-methoxybenzeneHCID 90455719—
CatalystTetrabutylammonium ChlorideHCID 70681—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
Product3-(5-Bromo-4-chloro-2-methoxyphenyl)propanalHCID 11760718734%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 1-bromo-2-chloro-5-iodo-4-methoxybenzene (3.2 g, 9.2 mmol), prop-2-en-1-ol (1.3 g, 23.0 mmol), Pd(OAc)2 (206 mg, 0.9 mmol), TBAC (2.56 g, 9.2 mmol), NaHCO3 (2.3 g, 27.6 mmol) in DMF (50 mL) was stirred under Argon at 60° C. for 16 h. The mixture was allowed to cool to RT, and then partitioned between ethyl acetate and water. The combined organic layer was washed with brine, dried over anhydrous Na2SO4 and concentrated. The residue was purified by flash column chromatography on silica gel (ethyl acetate/petroleum ether=1:20) to afford the desired product (860 mg, 34% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227978B2
Source datasetuspto-grants-2016_01
ORD IDord-199a28c7717345d09e3da49099e2d18d
Source noteuspto-grants-2016_01