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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 616996Generated: October 30, 2026

Potassium Iodide → 8-[4,4-Bis(p-fluorophenyl)cyclohexyl]-1-(p-fluorophenyl)-1,3,8-triazaspiro[4.5]decan-4-one

https://huagongshe.com/reaction/616996

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantDiisopropyl EtherHCID 7914—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(4-Fluorophenyl)-1,3,8-triazaspiro(4.5)decan-4-oneHCID 93915—
Reactant4,4-Bis(p-fluorophenyl)cyclohexyl mesylateHCID 20366885—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product8-[4,4-Bis(p-fluorophenyl)cyclohexyl]-1-(p-fluorophenyl)-1,3,8-triazaspiro[4.5]decan-4-oneHCID 13364151—

Reaction Steps

A mixture of 16 g of 4,4-bis(p-fluorophenyl)cyclohexyl mesylate, 10 g of 1-(p-fluorophenyl)-1,3,8-triazaspiro[4.5]decan-4-one (m.p. 234°-234.5° C), 6.1 g of potassium carbonate, 7.3 g of potassium iodide and 100 ml of dimethylformamide is stirred at 70°-80° C for 50 hours. The reaction mixture is poured into water, isopropyl ether is added to the aqueous mixture, and the resulting mixture is stirred for some time. The precipitated crystals are collected by filtration and dissolved in a mixture of chloroform and methanol (9:1). The solvent is removed to some degree and cooled in an ice bath. The precipitated crystals are collected by filtration and purified in the same manner to give 8-[4,4-bis(p-fluorophenyl)cyclohexyl]-1-(p-fluorophenyl)-1,3,8-triazaspiro[4.5]decan-4-one as white crystals, melting at 237°-240° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04076821
Source datasetuspto-grants-1978_02
ORD IDord-ff2233a8833a477bb5ba29a4969d5d31
Source noteuspto-grants-1978_02