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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1902676Generated: November 1, 2026

Potassium Iodide → N,N-diphenyl-4-[3-methylphenyl]-1-piperidinepropanamine butenedioate

https://huagongshe.com/reaction/1902676

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium CarbonateHCID 10340—
Reactant3-(N,N-diphenylamino)-1-chloropropaneHCID 10658053—
Reactant4-(3-Methylphenyl)piperidine hydrochlorideHCID 21936967—
ReactantN,N-diphenyl-4-[3-methylphenyl]-1-piperidinepropanamine butanedioateHCID 86738711—
Solvent1-ButanolHCID 263—
ProductN,N-diphenyl-4-[3-methylphenyl]-1-piperidinepropanamine butenedioateHCID 70530333—

Reaction Steps

A mixture of 7.37 g. (0.030 moles) of 3-[N,N-diphenylamino]-1-chloropropane, 6.0 g. (0.024 moles) of 4-(3-methylphenyl)-piperidine hydrochloride, 3.92 g. (0.024 moles) of potassium iodide, and 5.30 g. (0.050 moles) of sodium carbonate in 60 ml. of n-butanol is refluxed for about 16 hours. Solvent is evaporated and the residue is dissolved in chloroform and washed with water. The chloroform solution is dried and passed through a column of silica gel. The product is eluted with acetonitrile. The product fractions are combined, concentrated, and converted to the maleate salt in ether. The resulting crystals recrystallized from acetonitrile to give 7.2 g. of N,N-diphenyl-4-[3-methylphenyl]-1-piperidinepropanamine butanedioate (1:1), mp. 137.5°-139.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04364954
Source datasetuspto-grants-1982_12
ORD IDord-e51816231e014e4ea3646c46d7142062
Source noteuspto-grants-1982_12