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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587632Generated: October 30, 2026

4-Phenylpiperidine → 2,3-Dichloro-4-(4-phenyl-1-piperidinyl)pyridine

https://huagongshe.com/reaction/587632

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PhenylpiperidineHCID 69873—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
Reactant2,3-Dichloro-4-iodopyridineHCID 44887038—
SolventAcetonitrileHCID 6342—
Product2,3-Dichloro-4-(4-phenyl-1-piperidinyl)pyridineHCID 57459597—

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of D10 (4 g, 14.605 mmol), 4-phenylpiperidine (3.532 g, 21.907 mmol) and DIPEA (5.088 ml, 29.209 mmol) in CH3CN (150 ml) was heated in a sealed tube at 110° C. for 16 h. The mixture was then treated with NaHCO3 (aqueous sat. solution). The resulting mixture was extracted with EtOAc. The organic layer was separated, dried (Na2SO4) and concentrated in vacuo. The crude product was purified by column chromatography (silica gel; DCM/7M solution of NH3 in MeOH/EtOAc gradient as eluent). The desired fractions were collected and concentrated in vacuo to yield intermediate compound D14 (2.32 g, 52%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09226930B2
Source datasetuspto-grants-2016_01
ORD IDord-a6872e7637da46149d7ee195ad3f539e
Source noteuspto-grants-2016_01