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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2243314Erstellt: 27. Oktober 2026

9-Oxofluorene-4-carboxylic acid → 4-(1H-benzimidazol-2-yl)-fluoren-9-one

https://huagongshe.com/reaction/2243314

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt9-Oxofluorene-4-carboxylic acidHCID 80361—
Edukt(2-Aminophenyl)amideHCID 86621027—
LösungsmittelAcetic AcidHCID 176—
Produkt4-(1H-benzimidazol-2-yl)-fluoren-9-oneHCID 59208194—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

In a 50-ml three-necked flask under an argon atmosphere, heat, at 80° C. for 2 hours, a solution of 3 g of the (2-amino-phenyl)amide of 9-oxo-9H-fluorene-4-carboxylic acid obtained in the preceding stage, in 150 ml of acetic acid. After cooling, the precipitate that formed is drained. After purification by silica gel flash chromatography, eluting with mixtures of dichloromethane and ethyl acetate (90-10 then 80-20 and finally 70-30 by volume), we obtain 1.73 g of 4-(1H-benzimidazol-2-yl)-fluoren-9-one in the form of a yellow powder, which is used as it is in the next stage, with the following characteristics:

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07674795B2
Quelldatensatzuspto-grants-2010_03
ORD IDord-91000b449a9f4adba18f981a768e6866
Quellennotizuspto-grants-2010_03