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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1751835Generated: October 28, 2026

Hexane → 4-(3-Oxobutyl)benzoic acid methyl ester

https://huagongshe.com/reaction/1751835

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactant3-Buten-2-olHCID 11716—
ReactantTriphenylphosphineHCID 11776—
ReactantMethyl 4-bromobenzoateHCID 12081—
Catalystpalladium(II) acetateHCID 167845—
SolventTriethylamineHCID 8471—
SolventEthyl AcetateHCID 8857—
Product4-(3-Oxobutyl)benzoic acid methyl esterHCID 1093264026.1%

Reaction Conditions

Temperature75 °C

Reaction Steps

To a solution of methyl-4-bromobenzoate (1.0 g, 4.65 mmol) in triethylamine (13 mL) was added 3-buten-2-ol (1 mL, 11.63 mmol), palladium (II) acetate (0.104 g, 0.465 mmol), and then triphenylphosphine (0.244 g, 0.93 mmol). The reaction was stirred in a 75° C. oil bath overnight under nitrogen atmosphere. Monitoring by TLC (3:1 hexane:ethyl acetate) showed the product and aryl bromide. The reaction was cooled to room temperature and then concentrated. Water was then added followed by extraction with ethyl acetate. The organic layer was washed with water and brine, dried over Na2SO4, filtered and concentrated. The crude product was purified by flash column chromatography (5:1 to 3:1 hexane:ethyl acetate) to obtain the product (250 mg, 26% yield). 1H NMR (600 MHz, CDCl3): δ 7.95 (d, 2H, J=8.4 Hz), 7.25 (d, 2H, J=8.4 Hz), 3.90 (s, 3H), 2.95 (t, 2H, J=7.45 Hz), 2.77 (t, 2H, J=7.68 Hz), 2.14 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09161997B2
Source datasetuspto-grants-2015_10
ORD IDord-431d31c9758d470abb88627a12c5c45f
Source noteuspto-grants-2015_10