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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243333Generated: October 30, 2026

9-Oxofluorene-4-carboxylic acid → HCID 67360611, compound

https://huagongshe.com/reaction/2243333

Reaction equation

Participants

RoleNameHCIDCharge
Reactant9-Oxofluorene-4-carboxylic acidHCID 80361—
ReactantHCID 86621033HCID 86621033—
SolventAcetic AcidHCID 176—
ProductHCID 67360611HCID 67360611—

Reaction Steps

A mixture of 3.0 g of (2-amino-4-chlorophenyl)amide of 9-oxo-9H-fluorene-4-carboxylic acid in 120 ml of glacial acetic acid is refluxed for 2.5 hours. Allow the mixture to return to room temperature and evaporate the reaction medium to dryness under vacuum. The residue is taken up with 75 ml of dichloromethane, and the organic phase is washed with twice 50 ml of a saturated solution of sodium bicarbonate, and 50 ml of a saturated solution of sodium chloride. After drying over magnesium sulphate, the organic phase is evaporated to dryness under vacuum. In this way, we obtain 3.12 g of 4-(6-chloro-1H-benzimidazol-2-yl)-9H-fluoren-9-one in the form of a beige foam with the following characteristics:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674795B2
Source datasetuspto-grants-2010_03
ORD IDord-4fe8279d4dc2419e8ff2aaebeb5afead
Source noteuspto-grants-2010_03