HuagongsheHuagongshe Chemistry Print Report · For research reference only
9-Oxofluorene-4-carboxylic acid → HCID 67360611, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 9-Oxofluorene-4-carboxylic acid | HCID 80361 | — |
| Reactant | HCID 86621033 | HCID 86621033 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 67360611 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07674795B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-4fe8279d4dc2419e8ff2aaebeb5afead |
| Source note | uspto-grants-2010_03 |