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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1709902Generated: October 29, 2026

Potassium Iodide → 3-[3-[4-[Bis(4-fluorophenyl)hydroxymethyl]-1-piperidinyl]propoxy]-benzoic acid ethyl ester fumarate

https://huagongshe.com/reaction/1709902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium CarbonateHCID 10340—
ReactantFumaric AcidHCID 444972—
ReactantBis(4-fluorophenyl)(piperidin-4-yl)methanolHCID 11208889—
Reactant4-(Diphenylmethylene)-1-(3-phenoxypropyl)piperidine oxalateHCID 23036335—
Reactant3-(3-Chloro-propoxy)-benzoic acid ethyl esterHCID 54051377—
SolventDimethylformamideHCID 6228—
Product3-[3-[4-[Bis(4-fluorophenyl)hydroxymethyl]-1-piperidinyl]propoxy]-benzoic acid ethyl ester fumarateHCID 7037328967%

Reaction Steps

This compound was prepared according to the procedure used to synthesize the compound of Example 1. A mixture of 3.0 g (0.01 mole) of α, α-bis(p-fluorophenyl)-4-piperidinemethanol, 2.4 g (0.01 mole) of 3-(3-chloropropoxy)benzoic acid ethyl ester, 3.7 g (0.035 mole) of anhydrous sodium carbonate and 0.4 g of potassium iodide in 100 ml of dimethylformamide gave a gum as residue. The gum was converted to the fumaric acid salt and the solid was recrystallized from acetonitrile to yield 4.2 g (67%) of title compound as a fluffy,, white solid, mp 123°-131° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04950674
Source datasetuspto-grants-1990_08
ORD IDord-a069814467d74366b741b73f7ca7a979
Source noteuspto-grants-1990_08