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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382710Generated: November 1, 2026

Sodium Hydroxide → 1-Benzyl-4-methyl-4-phenylpiperidine

https://huagongshe.com/reaction/382710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant1-Benzyl-4-methylpiperidin-4-olHCID 10845913—
SolventBenzeneHCID 241—
Product1-Benzyl-4-methyl-4-phenylpiperidineHCID 10801662104%

Reaction Steps

1-Benzyl-4-methyl-piperidin-4-ol (4.81 g, 23.4 mmol, 1.00 equiv) was added to a suspension of AlCl3 (15.62 g, 117 mmol, 5.00 equiv) in benzene (100 mL) at room temperature under argon. The mixture was stirred at reflux for 24 hours, then cooled and poured cautiously into ice water (100 g of ice plus 50 mL of water). The aqueous phase was adjusted to pH 11-12 by addition of 6 N aqueous NaOH at 0° C., and extracted with EtOAc (3×100 mL). The combined organic solutions were dried over MgSO4 and concentrated. The residue was purified by flash chromatography (SiO2, hexane-Et2O 19:1 to 9:1 followed by hexane-EtOAc 3:1) to give 3.23 g (52%) of brown oil, which was characterized, spectroscopically.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06310076B1
Source datasetuspto-grants-2001_10
ORD IDord-cb7324df8aed4c1bab3962f4ef22d330
Source noteuspto-grants-2001_10