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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 381819Generated: October 25, 2026

4-Fluorobiphenyl → Methyl 4-(4'-fluoro-4-biphenylyl)-4-oxo-butyrate

https://huagongshe.com/reaction/381819

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorobiphenylHCID 9461—
ReactantButanoic acid, 4-chloro-4-oxo-, methyl esterHCID 73888—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
ProductMethyl 4-(4'-fluoro-4-biphenylyl)-4-oxo-butyrateHCID 1554112074.6%

Reaction Steps

To a stirred suspension of anhydrous aluminum chloride (9.64 g, 0.723 mol) in dichloromethane (90 mL) at 5° C. was added dropwise a solution of 4-fluorobiphenyl (4.97 g, 0.0289 mol) in dichloromethane (40 mL) followed by the dropwise addition of a solution of 3-carbomethoxypropionyl chloride (3.94 mL, 0.032 mol) in dichloromethane (30 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 (160 mL). The layers were separated, and the organic layer washed with brine, dried (Na2SO4), and rotary evaporated. The residue was recrystallized from methanol (300 mL) to give 6.17 g of 4-(4′-fluoro-biphenyl-4-yl)-4-oxo-butyric acid, methyl ester as a pale yellow solid; mp 131.5-133.0° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06307089B2
Source datasetuspto-grants-2001_10
ORD IDord-e554754d25da4b91b1ad3a91d61b2761
Source noteuspto-grants-2001_10