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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2103333Generated: October 29, 2026

Hydrochloric Acid → 4-(3-Fluorophenyl)butanoic acid

https://huagongshe.com/reaction/2103333

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantMethyl 4-(3-fluorophenyl)-4-oxobutanoateHCID 12465650—
SolventEthylene GlycolHCID 174—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product4-(3-Fluorophenyl)butanoic acidHCID 1491511375.3%

Reaction Steps

A solution of 4-(3-fluoro-phenyl)-4-oxo-butyric acid methyl ester (28.27 g, 134.49 mmol), hydrazine monohydrate (26.1 mL, 26.93 g, 537.96 mmol) and KOH (22.64 g, 403.47 mmol) in ethylene glycol (150 mL) was heated to reflux under argon and refluxed for 2 hours. The reaction mixture was cooled and diluted with 1.5 litres of water, 500 mL of Et2O was added, and the mixtures was acidified by addition of 6 M HCl with stirring, after which an additional 500 mL of Et2O was added. The organic layer was removed and the aqueous layer was extracted twice with 250 mL of 500 mL of Et2O/EtOAc (3:1). The combined organic layers were washed with water, saturated brine, and then dried over MgSO4. The solvent was evaporated under reduced pressure to yield a brownish oil, which was eluted through silica gel using hexanes/EtOAc (9:1). Removal of solvent under reduced pressure yielded 18.44 g (101.21 mmol, 75.26%) of 4-(3-fluoro-phenyl)-butyric acid as an oil. MS: 183 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576103B2
Source datasetuspto-grants-2009_08
ORD IDord-68a29ab0bc6f4499a96cb78b711a60c7
Source noteuspto-grants-2009_08