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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1979765Generated: October 29, 2026

Sodium Chloride → 1-(3-Chloropropyl)-4-phenylpiperidine

https://huagongshe.com/reaction/1979765

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantTriethylamineHCID 8471—
Reactant4-PhenylpiperidineHCID 69873—
SolventDimethylformamideHCID 6228—
Product1-(3-Chloropropyl)-4-phenylpiperidineHCID 203689—

Reaction Steps

24 Grams of 4-phenylpiperidine, 24 g of 1-chloro-3-bromopropane and 15 g of triethylamine were mixed with 100 ml of dimethylformamide and stirred at 50°-60° C. for 1 hour. The reaction mixture was poured into 200 ml of saturated sodium chloride aqueous-solution and the organic layer was extracted with chloroform. Then the chloroform layers was washed with water, dried and the chloroform was removed by distillation. The residue thus obtained was purified by a silica-gel column chromatography (to obtain only the main product at the upper-most portion in the column). 15.3 Grams of 1-chloro-3-(4-phenylpiperidinyl)propane was obtained as in the form of colorless oily substance. Then this oily substance was distilled under a reduced pressure to obtain 11 g of a fraction of distillate having the boiling point of 112°-115° C. (0.1 mmHg). A part of this distillate was made as in the form of hydrochloride and recrystallized from ethanol to obtain 1-chloro-3-(4-phenyl-1-piperidyl)propane monohydrochloride having the melting point of 167°-169° C. as in the form of colorless needle-like crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04482560
Source datasetuspto-grants-1984_11
ORD IDord-a6e200d02939473886ec8959476baf5e
Source noteuspto-grants-1984_11