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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1709910Generated: October 30, 2026

Potassium Iodide → HCID 23036407, compound

https://huagongshe.com/reaction/1709910

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium CarbonateHCID 10340—
ReactantBis(4-fluorophenyl)(piperidin-4-yl)methanolHCID 11208889—
ReactantHCID 23036325HCID 23036325—
Reactant4-(Diphenylmethylene)-1-(3-phenoxypropyl)piperidine oxalateHCID 23036335—
Solvent1-ButanolHCID 263—
SolventDiethyl EtherHCID 3283—
ProductHCID 23036407HCID 2303640717%

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, 2.8 g (0.01 mole) of 1-[4-(4-chlorohexyloxy)-3-methoxyphenyl]ethanone, 5.3 g (0.05 mole) of anhydrous sodium carbonate and 0.3 g of potassium iodide in 100 ml of 1-butanol gave a gum as resiude. The gum was purified by column chromatography on 80 g of Florisil®. Fractions eluted with 2-5% acetone in benzene were combined and concentrated to give a glass as residue. The glass was dissolved in anhydrous ethyl ether, filtered and the filtrate treated with ethereal hydrogen chloride. A gummy solid precipitated. This solid was triturated with fresh ethyl ether until a fine, white solid resulted. The solid was collected by filtration and dried to yield 1.0 g (17%) of title compound as a white solid, mp 182°-186° C. with decomposition.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04950674
Source datasetuspto-grants-1990_08
ORD IDord-512bcf8cef3b4ad7b0d0a02d3ca030e4
Source noteuspto-grants-1990_08