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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73843Generated: October 30, 2026

1-[(4-Fluorobenzoyl)amino]cyclohexanecarboxylic acid → 2-(4-Fluorophenyl)-3-oxa-1-azaspiro[4.5]dec-1-en-4-one

https://huagongshe.com/reaction/73843

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-[(4-Fluorobenzoyl)amino]cyclohexanecarboxylic acidHCID 24693962—
SolventAcetic AnhydrideHCID 7918—
Product2-(4-Fluorophenyl)-3-oxa-1-azaspiro[4.5]dec-1-en-4-oneHCID 5767289469%

Reaction Conditions

Temperature100 °C

Reaction Steps

After a suspension of 13.3 g (50 mmol) of 1-[(4-fluorobenzoyl)amino]cyclohexanecarboxylic acid in 30 ml of acetic anhydride was stirred at 100° C. for 30 minutes, the reaction solution was concentrated under reduced pressure. Toluene was added to the residue, and the mixture was washed with water, a saturated aqueous sodium hydrogencarbonate solution and then saturated brine. After the organic layer was dried with anhydrous sodium sulfate, the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography to obtain 8.5 g (69%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829209B2
Source datasetuspto-grants-2014_09
ORD IDord-0b553825e7b743cb99245ba8d4ddb88c
Source noteuspto-grants-2014_09