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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2259924Generated: November 1, 2026

Benzyl Chloride → N-Benzyl-4-Acetyl4-(4-Chlorobenzyl)-piperidine

https://huagongshe.com/reaction/2259924

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ChlorideHCID 7503—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 19962172HCID 19962172—
SolventAcetonitrileHCID 6342—
ProductN-Benzyl-4-Acetyl4-(4-Chlorobenzyl)-piperidineHCID 1996217498.8%

Reaction Steps

A suspension of 4-Acetyl-4-(4-chlorobenzyl)-piperidine hydrochloride (0.600 g, 2.09 mmol) in acetonitrile (20 mL) was treated with solid sodium bicarbonate (200 mg, xs) and benzyl chloride (292 mg, 2.3 mol) and heated to reflux for 3 hours. The reaction was then cooled to room temperature, poured into saturated aqueous sodium bicarbonate (200 mL) and extracted with ethyl acetate (3×100 mL). The combined extracts were dried over anhydrous magnesium sulfate, filtered, and concentrated at reduced pressure. The residue was chromatographed on silica gel eluting with 2% Methanol/chloroform to give 706 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05475109
Source datasetuspto-grants-1995_12
ORD IDord-17b469b3302549939eb0fba6deb9b643
Source noteuspto-grants-1995_12