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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382661Generated: November 1, 2026

Benzene → 4-Phenylpiperidine

https://huagongshe.com/reaction/382661

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 numberUS06310076B1
Source datasetuspto-grants-2001_10
ORD IDord-3c2b7d8ff6a449eb902d980d93559629
Source noteuspto-grants-2001_10