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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2235560Erstellt: 25. Oktober 2026

1-Ethylcyclopentene → 7-(2-Ethyl-1-piperidinyl)-1-methyl-1,3-dihydro-2H-benzimidazol-2-one

https://huagongshe.com/reaction/2235560

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-EthylcyclopenteneHCID 137448—
EduktSodium BicarbonateHCID 516892—
Edukt7-Amino-1-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-oneHCID 59635419—
EduktHCID 178418361HCID 178418361—
KatalysatorPalladiumHCID 23938—
LösungsmittelMethanolHCID 887—
Produkt7-(2-Ethyl-1-piperidinyl)-1-methyl-1,3-dihydro-2H-benzimidazol-2-oneHCID 6858109675%

Reaktionsschritte

A mixture of 1-ethylcyclopentene (1.0 g, 10.4 mmol) and sodium bicarbonate (0.1 g, 1.19 mmol) in methanol (150 ml) was ozonized at −78° C. until TLC analysis indicated complete consumption of 1-ethylcyclopentene. The crude ozonide was transferred directly to a mixture of 7-amino-1-methyl-1,3-dihydro-2H-benzimidazol-2-one (0.5 g, 3.07 mmol) and 10% palladium on carbon (0.05 g, Degussa type; 50% wet). The flask was fitted with a balloon of hydrogen and allowed to stir for 12 h. The reaction was filtered through GF/F paper and the filtrate concentrated under reduced pressure. The residue was purified by column chromatography eluting with a 10% acetone/hexanes mixture to afford 597 mg (75%) of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07714009B2
Quelldatensatzuspto-grants-2010_05
ORD IDord-067988451bd74655a05dd717b5b777b4
Quellennotizuspto-grants-2010_05