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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1747727Generated: October 31, 2026

Sulfuric Acid → 1-(4-Fluorophenyl)-3-methyl-1-butanone

https://huagongshe.com/reaction/1747727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactant4-FluorobenzonitrileHCID 14517—
ReactantHCID 178418368HCID 178418368—
SolventDiethyl EtherHCID 3283—
Product1-(4-Fluorophenyl)-3-methyl-1-butanoneHCID 2064462042%

Reaction Steps

To a solution of 4-fluoro-benzonitrile (6 g, 49.5 mmol) in diethyl ether (200 mL) was added i-BuMgCl (1 M soln in THF) and the reaction mixture heated to reflux for 16 hours. The reaction mixture was cooled to room temperature and poured into a mixture 6 N H2SO4 (60 mL) and ice (500 mL), then stirred at 0° C. for 30 min. The aqueous layer was extracted with ethyl acetate (200 mL), the combined organic layers were washed with brine (100 mL), dried (MgSO4), and concentrated. The residue was purified by column chromatography (80 g, SiO2, 0 to 40% diethyl ether/dichloromethane 1:1 in hexanes) to provide 1-(4-fluorophenyl)-3-methylbutan-1-one as a colorless oil (3.72 g, 42%): 1H NMR (300 MHz, CHLOROFORM-d) δ ppm 1.00 (d, J=6.78 Hz, 6H), 2.29 (dt, J=13.47, 6.64 Hz, 1H), 2.81 (d, J=6.78 Hz, 2H), 7.06-7.19 (m, 2H), 7.94-8.02 (m, 2H); MS m/z 172 (Dimer-OH)++.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150582B2
Source datasetuspto-grants-2015_10
ORD IDord-24888662d0a648df97902b1a24c5e89e
Source noteuspto-grants-2015_10