Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1902671Generated: October 31, 2026

Sodium Iodide → 1-[3-(Diphenylamino)propyl]-4-(3-fluorophenyl)-4-piperidinol ethanedioate

https://huagongshe.com/reaction/1902671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantMethyl Ethyl KetoneHCID 6569—
ReactantSodium CarbonateHCID 10340—
Reactant3-[N,N-diphenylamino)-1-bromopropaneHCID 10827329—
Reactant4-(3-Fluorophenyl)piperidin-4-olHCID 12763906—
Product1-[3-(Diphenylamino)propyl]-4-(3-fluorophenyl)-4-piperidinol ethanedioateHCID 86738023—

Reaction Steps

A mixture of 10.4 g. (0.018 moles) of 3-[N,N-diphenylamino]-1-bromopropane, 3.5 g. (0.018 moles) of 4-(3-fluorophenyl)-4-piperidinol, 1.9 g. (0.018 moles) of sodium carbonate and 1.0 g. of sodium iodide in 100 ml. of methyl ethyl ketone is refluxed for about 3 hours. The reaction is allowed to cool, filtered and the filtrate is evaporated. The residue is shaken with a mixture of diethyl ether and dilute hydrochloric acid. An oily third phase forms which crystallizes on scratching. This material is recrystallized from isopropanol and then from ethanol, and converted back to the free base. The product is then crystallized from isopropanol containing an excess of oxalic acid giving 2.2 g. of 1-[3-(diphenylamino)propyl]-4-(3-fluorophenyl)-4-piperidinol ethanedioate (1:1), mp. 181°-182.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04364954
Source datasetuspto-grants-1982_12
ORD IDord-5242efcf837f40d1816fd3231860f0a6
Source noteuspto-grants-1982_12