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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1709911Generated: October 31, 2026

Potassium Iodide → 4-[4-[4-[Bis(4-fluorophenyl)hydroxymethyl]-1-piperidinyl]butoxy]benzoic acid methyl ester fumarate

https://huagongshe.com/reaction/1709911

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium CarbonateHCID 10340—
ReactantFumaric AcidHCID 444972—
ReactantBis(4-fluorophenyl)(piperidin-4-yl)methanolHCID 11208889—
ReactantMethyl 4-(4-chlorobutoxy)benzoateHCID 14575308—
Reactant4-(Diphenylmethylene)-1-(3-phenoxypropyl)piperidine oxalateHCID 23036335—
SolventDimethylformamideHCID 6228—
Product4-[4-[4-[Bis(4-fluorophenyl)hydroxymethyl]-1-piperidinyl]butoxy]benzoic acid methyl ester fumarateHCID 7037343265%

Reaction Steps

This compound was prepared according to the procedure used to synthesize the compound of Example 1. A mixture of 9.1 g (0.03 mole) of α,α-bis(p-fluorophenyl)-4-piperidinemethanol, 7.3 g (0.03 mole) of 4-(4-chlorobutoxy)benzoic acid methyl ester, 10.6 g (0.1 mole) of anhydrous sodium carbonate and 0.5 g of potassium iodide in 125 ml of dimethylformamide gave a gum as residue. The gum was converted to the fumaric acid salt and the solid was recrystallized from acetonitrile-dimethylformamide to yield 12.2 g (65%) of title compound as a white solid, mp 186°-188° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04950674
Source datasetuspto-grants-1990_08
ORD IDord-28ca881b34754dd1a5d6181e1ce5c106
Source noteuspto-grants-1990_08