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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369907Generated: October 29, 2026

Water → (2R)-2-[(1R)-3,3-difluorocyclopentyl]-2-hydroxy-2-phenylacetic acid

https://huagongshe.com/reaction/369907

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantPyridine, hydrofluoride (1:1)HCID 64774—
ReactantNitrilooxonium tetrafluoroborateHCID 11137142—
Reactant(2R,5R)-2-(t-butyl)-5-((1R)-3-hydroxyiminocyclopentyl)-5-phenyl-1,3-dioxolan-4-oneHCID 86754451—
SolventDichloromethaneHCID 6344—
Product(2R)-2-[(1R)-3,3-difluorocyclopentyl]-2-hydroxy-2-phenylacetic acidHCID 10890505—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of 20 mg of nitrosonium tetrafluoroborate in 0.5 ml of 70% hydrogen fluoride-pyridine, a solution of 34 mg of (2R,5R)-2-(t-butyl)-5-((1R)-3-hydroxyiminocyclopentyl)-5-phenyl-1,3-dioxolan-4-one in 0.5 ml of dichloromethane was added under cooling with ice, followed by stirring for 10 minutes at 0° C. and for 5 hours at room temperature. Water was added to the reaction mixture under cooling with ice, and extraction was carried out with ethyl acetate. After sequential washing with a saturated aqueous solution of sodium hydrogencarbonate and brine, the organic layer was dried over anhydrous magnesium sulfate. Distilling the solvent off under reduced pressure gave 35 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06140333
Source datasetuspto-grants-2000_10
ORD IDord-a5627e87915e4aac8f46ff7e9149549d
Source noteuspto-grants-2000_10