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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1059065Generated: October 26, 2026

4-Isobutylbenzoic acid → (4-Isobutylphenyl)(phenyl)methanone

https://huagongshe.com/reaction/1059065

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Isobutylbenzoic acidHCID 38111—
ReactantOxalyl chlorideHCID 65578—
ReactantAluminum(III) ChlorideHCID 6451240—
CatalystDimethylformamideHCID 6228—
SolventBenzeneHCID 241—
SolventDichloromethaneHCID 6344—
Product(4-Isobutylphenyl)(phenyl)methanoneHCID 1215828681%

Reaction Steps

A solution of 4-isobutylbenzoic acid (5.00 g, 28.0 mmol) in CH2Cl2 was cooled in an ice bath and treated with oxalyl chloride (5 mL) and DMF (1 drop). The mixture was warmed to room temp and stirred 1 h. The volatiles were removed in vacuo to give the crude acid chloride which as dissolved in benzene (50 mL). Aluminum chloride (4.49 g, 33.3 mmol) was added and the mixture was heated to reflux for 3.5 h. The mixture was cooled to room temp and then poured onto ice (ca. 100 g). The mixture was extracted with EtOAc (3×100 mL) and the combined organic extracts were washed with ½ satd aqueous NaHCO3 (100 mL), dried (Na2SO4), filtered and evaporated in vacuo. The resulting residue was purified by silica gel chromatography (elute with 10:1 hexane/EtOAc) to give 4-isobutylbenzophenone (5.48 g, 81%). 1H NMR (CDCl3) 7.75 (m, 4H), 7.53 (d, 1H), 7.47 (t, 2H), 7.23 (d, 2H), 2.53 (d, 2H), 1.91 (m, 1H), 0.92 (d, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06518424B1
Source datasetuspto-grants-2003_02
ORD IDord-48936313db894300b798028ea9202c83
Source noteuspto-grants-2003_02