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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 46902Erstellt: 24. Oktober 2026

Potassium Iodide → 8-[3-(1H-benzimidazol-1-yl)propyl]-1-phenyl-1,3,8-triazaspiro[4,5]decan-4-one

https://huagongshe.com/de/reaction/46902

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium IodideHCID 4875—
EduktSodium CarbonateHCID 10340—
Edukt1-Phenyl-1,3,8-triazaspiro(4.5)decan-4-oneHCID 70556—
Edukt1-(3-Chloropropyl)-1H-benzimidazoleHCID 13105517—
LösungsmittelWaterHCID 962—
LösungsmittelMethyl Isobutyl KetoneHCID 7909—
Produkt8-[3-(1H-benzimidazol-1-yl)propyl]-1-phenyl-1,3,8-triazaspiro[4,5]decan-4-oneHCID 2038563925%

Reaktionsschritte

A mixture of 6 parts of 1-(3-chloropropyl)-1H-benzimidazole, 4.6 parts of 1-phenyl-1,3,8-triazaspiro[4,5]decan-4-one, 10 parts of sodium carbonate, 0.1 parts of potassium iodide and 80 parts of 4-methyl-2-pentanone is stirred and refluxed overnight. The reaction mixture is cooled, water is added and the layers are separated. The organic phase is dried, filtered and evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (90:10 by volume) as eluent. The pure fractions are collected and the eluent is evaporated. The residue is crystallized from 4-methyl-2-pentanone, yielding 2parts (25%) of 8-[3-(1H-benzimidazol-1-yl)propyl]-1-phenyl-1,3,8-triazaspiro-[4,5]decan-4-one; mp. 191° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04175129
Quelldatensatzuspto-grants-1979_11
ORD IDord-d97cbc76753b4a4eba775885524be3cb
Quellennotizuspto-grants-1979_11