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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9519Generated: October 25, 2026

Bromobenzene → 4-(4-Bromophenyl)-2,2-dimethyl-4-oxo-butyric Acid

https://huagongshe.com/reaction/9519

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromobenzeneHCID 7961—
Reactant2,2-Dimethylsuccinic anhydrideHCID 87067—
ReactantAluminumHCID 5359268—
Solvent1,1-DichloroethaneHCID 6365—
Product4-(4-Bromophenyl)-2,2-dimethyl-4-oxo-butyric AcidHCID 2198575763%

Reaction Steps

To a chilled solution (ice/water bath) of bromobenzene (7.71 g, 49.1 mmol) and 3,3-dimethyldihydro-2,5-furandione (5.99 g, 46.7 mmol) in dichloroethane (150 mL) was added aluminum trichworide (13.28 g, 99.58 mmol). The ice bath was removed and the reaction mixture was stirred at rt overnight. The mixture was again chilled in an ice/water bath, and then quenched with 1 M aqueous hydrochloric acid. Water (70 mL) was added and the layers were separated. The aqueous layer was extracted with ethyl acetate (3×50 mL). The combined organic layers were dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by flash chromatography (Biotage apparatus, 17:83 ethyl acetate/hexane) to give 4-(4-bromophenyl)-2,2-dimethyl-4-oxobutanoic acid as a white solid (8.34 g, 63%). LC-MS: ret. time 2.79 min; m/z 284.8 (MH+); 1H NMR (300 MHz, CDCl3) δ 1.36 (s, 6H), 3.27 (s, 2H), 7.60 (d, 2H), 7.81 (d, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091228B2
Source datasetuspto-grants-2006_08
ORD IDord-df37945b51904d399bb64ad4006d4aeb
Source noteuspto-grants-2006_08