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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243314Generated: October 25, 2026

9-Oxofluorene-4-carboxylic acid → HCID 59208194, compound

https://huagongshe.com/reaction/2243314

Reaction equation

Participants

RoleNameHCIDCharge
Reactant9-Oxofluorene-4-carboxylic acidHCID 80361—
ReactantHCID 86621027HCID 86621027—
SolventAcetic AcidHCID 176—
ProductHCID 59208194HCID 59208194—

Reaction Conditions

Temperature80 °C

Reaction Steps

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:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674795B2
Source datasetuspto-grants-2010_03
ORD IDord-91000b449a9f4adba18f981a768e6866
Source noteuspto-grants-2010_03