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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 381816Generated: October 31, 2026

4-Bromobiphenyl → HCID 15541117, compound

https://huagongshe.com/reaction/381816

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromobiphenylHCID 7101—
ReactantButanoic acid, 4-chloro-4-oxo-, methyl esterHCID 73888—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
ProductHCID 15541117HCID 1554111777.2%

Reaction Steps

To a stirred suspension of anhydrous aluminum chloride (3.45 g, 0.026 mol) in dichloromethane (20 mL) at 5° C. was added dropwise a solution of 4-bromobiphenyl (2.3 g, 0.010 mol) in dichloromethane (11 mL) followed by the dropwise addition of 3-carbomethoxypropionyl chloride (1.35 mL, 0.011 mol) in dichloromethane (15 mL), and the mixture stirred. After 2 hours at 5° C., the mixture was allowed to warm to room temperature. After 1 day, the reaction was cooled to 5° C. and quenched by the dropwise addition of water (50 mL). The layers were separated, and the organic layer washed with water and brine, dried (MgSO4), and rotary evaporated. The residue was dissolved (CH2Cl2) and purified by column chromatography on silica gel, eluting with dichloromethane to give 2.68 g of 4-(4′-bromo-biphenyl-4-yl)-4-oxo-butyric acid, methyl ester as a white solid; mp 115.0-116.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06307089B2
Source datasetuspto-grants-2001_10
ORD IDord-81286068ecd2459c9b0f5f1054bb056f
Source noteuspto-grants-2001_10