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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 326008Generated: October 29, 2026

Potassium Hydroxide → 2-[(4-Fluorophenyl)methyl]heptanedioic acid

https://huagongshe.com/reaction/326008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant4-Fluorobenzyl bromideHCID 68021—
ReactantEthyl 2-oxocyclohexanecarboxylateHCID 95543—
ReactantSodium ethoxideHCID 2723922—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product2-[(4-Fluorophenyl)methyl]heptanedioic acidHCID 1351976987.6%

Reaction Steps

19.2 g of 2-oxocyclohexanecarboxylic acid ethyl ester, 21.4 g of p-fluorobenzyl bromide, 7.7 g of sodium ethoxide and 200 ml of ethanol were mixed together to form a mixture which was refluxed for 2 hours, incorporated with 500 ml of water and subjected to extraction with ethyl ether. The resulting ether layer was freed of the ether to obtain a residue. The thus obtained residue was dissolved in 500 ml of 70% ethanol, incorporated with 16.1 g of potassium hydroxide, refluxed for 3 hours and hydrolyzed to obtain 26.5 g of 1-(4-fluorobenzyl)-1,5-pentane dicarboxylic acid having a melting point of 80°-81° C. in the colorless needle form. 26 g of the thus obtained compound in the needle form and 300 g of polyphosphoric acid were mixed together to form a mixture which was agitated at 100° C. for 3 hours. After the end of the reaction, the resulting reaction mixture was incorporated with iced water and subjected to extraction with ethyl acetate. The organic layer was washed with water, dehydrated and freed of the solvent by distilling it off, thereby to obtain a residue. The thus obtained residue was recrystallized from isopropyl ether to obtain 18.2 g of 6-fluoro-1-oxo-2,3-dihydro-2-indene valeric acid in the colorless platy form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04443626
Source datasetuspto-grants-1984_04
ORD IDord-8c2c92b7eb6048f18bafb815685ead19
Source noteuspto-grants-1984_04