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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491403Generated: October 31, 2026

Water → Methyl 5-(3-oxopropyl)furan-2-carboxylate

https://huagongshe.com/reaction/491403

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAllyl AlcoholHCID 7858—
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl 5-bromofuran-2-carboxylateHCID 599633—
CatalystTetrabutylammonium ChlorideHCID 70681—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductMethyl 5-(3-oxopropyl)furan-2-carboxylateHCID 1241256428.1%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of 5-bromo-2-furancarboxylic acid methyl ester (816 mg, MAYB) in DMF (3 ml) was added with tetra-n-butylammonium chloride (1.1 g, TCI), sodium hydrogencarbonate (688 mg), palladium acetate (10.4 mg, WAKO), and allyl alcohol (346 mg, TCI), and the mixture was stirred at 60° C. for 20 hours. The reaction solution was added with distilled water (30 ml), and ethyl acetate (20 ml), and the insoluble solid was removed by filtration. The filtrate was extracted with ethyl acetate (50 ml×2). The organic layers were combined, washed with saturated brine, and dried, and then the filtrate was concentrated under reduced pressure. The residue was purified by column chromatography (Flash, hexane:ethyl acetate=4:1) to obtain the title compound (Intermediate ih-01, 204 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531533B2
Source datasetuspto-grants-2009_05
ORD IDord-9400ccdb69da490ba630e83494046cda
Source noteuspto-grants-2009_05