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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256776Generated: October 30, 2026

Sulfuric Acid → 5-(2-Fluoro-4-biphenylyl)-4-oxohexanoic acid

https://huagongshe.com/reaction/256776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantDiethyl 2-(3-(2-fluoro-4-biphenylyl)-2-oxobutyl)malonateHCID 19785556—
SolventAcetic AcidHCID 176—
Product5-(2-Fluoro-4-biphenylyl)-4-oxohexanoic acidHCID 1978556654%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of diethyl 2-(3-(2-fluoro-4-biphenylyl)-2-oxobutyl)malonate (5.00 g, 12.5 mmoles), acetic acid (100 ml), and 30% sulfuric acid (100 ml) was heated under reflux for 4 hours. After cooling the reaction mixture was extracted with ether. The organic layer was washed with water, dried over sodium sulfate and concentrated under reduced pressure The mixture of the residue, ethanol (100 ml) and concentrated sulfuric acid (1.0 g) was heated at 50° C. for 3 hours. The reaction mixture was concentrated under reduced pressure and the residue was extracted with ether. The organic layer was washed successively with water, aqueous sodium bicarbonate and water, dried over sodium sulfate and concentrated under reduced pressure. Purification of the residue by medium pressure silica gel column chromatography gave the desired 5-(2-fluoro-4-biphenylyl)-4-oxohexanoic acid (2.21 g, 6.71 mmoles, yield 54%) as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05258396
Source datasetuspto-grants-1993_11
ORD IDord-0b5cb571e7dc4a5d9c8111adbf6c6bdd
Source noteuspto-grants-1993_11