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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 396605Generated: October 30, 2026

Benzene → 4-Phenylpiperidine

https://huagongshe.com/reaction/396605

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantSodium HydroxideHCID 14798—
ReactantPiperidin-4-olHCID 79341—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventWaterHCID 962—
Product4-PhenylpiperidineHCID 6987340%

Reaction Steps

4-Hydroxypiperidine (10.0 g, 98.9 mmol, 1.00 equiv) and AlCl3 (105.5 g, 791.2 mmol, 8.0 equiv) were stirred in refluxing benzene (350 mL) under a CaSO4 drying tube for 85 hours. The mixture was cooled to room temperature and poured carefully into ice (500 g) and water (50 mL) with stirring. With ice water cooling, the pH was adjusted to 10-11 by addition of solid NaOH. The resulting mixture was extracted with EtOAc (3×250 mL). The combined organic solutions were washed with brine, dried over MgSO4, and concentrated to give 6.5 g of 4-phenylpiperidine (yellow solid, 40%), which was characterized spectroscopically.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06608086B2
Source datasetuspto-grants-2003_08
ORD IDord-f99334bf29a441918aca4e68186ab13c
Source noteuspto-grants-2003_08