Ammonia → 9H-fluorene-9-carboxamide
Reaction equation
[CH:1]1[C:13]2[CH:12]([C:14]([OH:16])=O)[C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[C:5]=2[CH:4]=[CH:3][CH:2]=1.C(Cl)(=O)C(Cl)=O.[NH3:23]>C1(C)C=CC=CC=1.CCOCC>[CH:1]1[C:13]2[CH:12]([C:14]([NH2:23])=[O:16])[C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[C:5]=2[CH:4]=[CH:3][CH:2]=1Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
The compound was prepared substantially in accordance with the procedure detailed in Example 21A, using 9-fluorenecarboxylic acid (6.00 g, 28.5 mmol) and oxalyl chloride (3.5 ml, 39.9 mmol) in 30 ml of toluene to provide a clear oil that was dissolved in Et2O and treated with ammonia.
Workup
- customThe compound was prepared substantially in accordance with the procedure
- customto provide a clear oil that
Sources & evidence
- ORD record
- ord-69ea179f45d340048ead38ed76bad320
- Source dataset
- uspto-grants-2000_05
- Patent number
- US06060484
Reaction notes
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