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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2421192Generated: November 4, 2026

4,4-Difluoropiperidine hydrochloride → HCID 16722359, compound

https://huagongshe.com/reaction/2421192

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,4-Difluoropiperidine hydrochlorideHCID 2758351—
ReactantSodium t-butoxideHCID 23676156—
ReactantHCID 67215624HCID 67215624—
SolventTolueneHCID 1140—
ProductHCID 16722359HCID 1672235970%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 2-(4-iodo-phenyl)-5-(5-methyl-3-phenyl-isoxazol-4-yl)-[1,3,4]oxadiazole (200 mg, 0.47 mmol) in toluene (2 mL) were added under an atmosphere of nitrogen 2-(dicyclohexylphosphino)biphenyl (15 mg, 0.04 mmol), tris(dibenzylideneacetone)di-palladium(0) chloroform complex (15 mg, 0.01 mmol), sodium tert-butoxide (107 mg, 1.12 mmol) and 4,4-difluoropiperidine hydrochloride (88 mg, 0.56 mmol). The reaction mixture was stirred for 1 h at 100° C. and was extracted with water (20 mL) and ethyl acetate (20 mL). The aqueous layer was extracted with ethyl acetate and the combined organic layers were washed with brine. Drying over sodium sulfate and purification by chromatography (SiO2, heptane:ethyl acetate=80:20 to 50:50) afforded the title compound (138 mg, 70%) as a light yellow solid. MS: m/e=423.3 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07956074B2
Source datasetuspto-grants-2011_06
ORD IDord-50ff7dbe168d4d61b365a38c0dbb9e9c
Source noteuspto-grants-2011_06