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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503182Generated: October 30, 2026

Diethyl Ether → 3-(3-fluorophenyl)butanoic acid

https://huagongshe.com/reaction/1503182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 58155375HCID 58155375—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product3-(3-fluorophenyl)butanoic acidHCID 1612615792.6%

Reaction Steps

A crude solution of 3-(3-fluorophenyl)butyric acid ethyl ester, 10.1 g, 48 mmol] in ethanol (50 mL) was treated with 10 M NaOH solution (50 mL, 857 mmol). The reaction mixture was refluxed overnight. The reaction mixture was dried under reduced pressure in order to get rid of the ethyl alcohol. The resulting residue was re-dissolved in 150 mL of water. The mixture was transferred to a separatory funnel using water (50 mL) and diethyl ether (200 mL). The mixture was equilibrated and the ether layer was removed. The aqueous layer was acidified by HCl solution (pH˜2) and extracted with diethyl ether (300 mL). The organic layer was dried over magnesium sulfate, filtered, and concentrated under reduced pressure. This afforded 8.1 g of an orange viscous oil, 3-(3-fluorophenyl)butyric acid (92.6% yield). This material was determined to be 100% pure by GC/MS analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212155B2
Source datasetuspto-grants-2015_12
ORD IDord-df7054600e1b443ea63a4a0bbe817343
Source noteuspto-grants-2015_12