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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437661Generated: October 27, 2026

Potassium Iodide → HCID 54236221, compound

https://huagongshe.com/reaction/437661

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant1-Phenyl-1,3,8-triazaspiro(4.5)decan-4-oneHCID 70556—
ReactantN-(2-Chloroethyl)-2-furamideHCID 182358—
SolventDimethylformamideHCID 6228—
ProductHCID 54236221HCID 54236221—

Reaction Steps

A member of 6.9 parts of N-(2-chloroethyl)-2-furancarboxamide, 9.2 parts of 1-phenyl-1,3,8-triazaspiro[4,5]decan-4-one, 6.6 parts of potassium iodide and 135 parts of N,N-dimethylformamide is stirred first for 3 hours at reflux and further overnight at room temperature. The reaction mixture is evaporated and the residue is taken up in water. The whole is alkalized and the product is extracted with 4-methyl-2-pentanone. The extract is dried, filtered and evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (96:4 by volume) as eluent. The pure fractions are collected and the eluent is evaporated. The solid residue is crystallized from 2-propanone. The product is filtered off and dried, yielding 1.9 parts of N-[2-(4-oxo-1-phenyl-1,3,8-triazaspiro [4,5]dec-8-yl)ethyl]-2-furancarboxamide; mp. 196.3° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04031226
Source datasetuspto-grants-1977_06
ORD IDord-4ab325a9b662424abdb147dbcfead2b4
Source noteuspto-grants-1977_06