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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1392831Generated: November 4, 2026

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

https://huagongshe.com/reaction/1392831

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 numberUS07344702B2
Source datasetuspto-grants-2008_03
ORD IDord-8ceccfba23dc404c9b3a1a84e587d769
Source noteuspto-grants-2008_03