Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 416020Generated: October 30, 2026

Water → (r)-1-Cyclohex-3-enyl-3-[3,5-dichloro-4'-(4-trifluoromethyl-piperidine-1-carbonyl)-biphenyl-4-ylmethyl]-pyrrolidin-2-one

https://huagongshe.com/reaction/416020

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTetrabutylammonium Fluoride TrihydrateHCID 11726816—
ReactantHCID 178505321HCID 178505321—
SolventAcetonitrileHCID 6342—
Product(r)-1-Cyclohex-3-enyl-3-[3,5-dichloro-4'-(4-trifluoromethyl-piperidine-1-carbonyl)-biphenyl-4-ylmethyl]-pyrrolidin-2-oneHCID 57741497—

Reaction Conditions

Temperature80 °C

Reaction Steps

Dissolve tetrabutylammonium fluoride trihydrate (0.436 g, 1.36 mmol) in 5 ml of acetonitrile. Add water (0.05 ml. 2.72 mmol) and stir for 10 minutes. Add trans-methanesulfonic acid 4-{(R)-3-[3,5-dichloro-4′-(4-trifluoromethyl-piperidine-1-carbonyl)-biphenyl-4-ylmethyl]-2-oxo-pyrrolidin-1-yl}-cyclohexyl ester (0.458 g, 0.68 mmol). Stir at 80° C. for 12 hours. Quench with saturated aqueous sodium bicarbonate and extract with ethyl acetate. Wash the extract with brine. Dry the organic layer over magnesium sulfate, filter, and concentrate under vacuum. Purify by silica gel chromatography recover 0.036 g (9%) of the title compound: MS (m/z): 579 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088776B2
Source datasetuspto-grants-2012_01
ORD IDord-dc2b596782074e8e8129166e1c3aa702
Source noteuspto-grants-2012_01