Acetic Acid → HCID 22561787, compound
Reaction equation
[F:1][C:2]1[CH:3]=[C:4]([C:9]2[CH:17]=[CH:16][CH:15]=[C:14]3[C:10]=2[CH:11]=[CH:12][NH:13]3)[CH:5]=[C:6]([F:8])[CH:7]=1.C([OH:20])C.C(O)(=O)C.[Br-].[Br-].[Br-].[NH+]1C=CC=CC=1.[NH+]1C=CC=CC=1.[NH+]1C=CC=CC=1>CC(O)(C)C.[Zn]>[F:1][C:2]1[CH:3]=[C:4]([C:9]2[CH:17]=[CH:16][CH:15]=[C:14]3[C:10]=2[CH2:11][C:12](=[O:20])[NH:13]3)[CH:5]=[C:6]([F:8])[CH:7]=1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
To the suspension of 4-(3,5-difluoro-phenyl)-1H-indole (13.52 g, 59 mmol) in t-BuOH:ethanol:acetic acid (375 mL:225 mL:115 mL) was added pyridinium tribromide (57 g, 177 mmol) portionwise. The mixture was stirred at room temperature for 3 hours, and then to the mixture was added with acetic acid (286 mL). Zinc dust (19.25 g, 295 mmol) was added to the reaction mixture portionwise. After stirring for one hour, any unreacted zinc was filtered off and most of the solvent was removed under reduced pressure. The residue was diluted with ethyl acetate, washed with water (5×), neutralized with 1N HCl, washed with sat. NaHCO3, brine, dried over Na2SO4, concentrated and triturated with ether to give 9.88 g (68%) of 4-(3,5-difluoro-phenyl)-1,3-dihydro-indol-2-one.
Workup
- stirringAfter stirring for one hour
- filtrationany unreacted zinc was filtered off and most of the solvent
- customwas removed under reduced pressure
- additionThe residue was diluted with ethyl acetate
- washwashed with water (5×)
- washwashed with sat. NaHCO3, brine
- dry with materialdried over Na2SO4
- concentrationconcentrated
- customtriturated with ether
Sources & evidence
- ORD record
- ord-9cb3317d69604564949d07ef6f719e1e
- Source dataset
- uspto-grants-2004_01
- Patent number
- US06677368B2
Reaction notes
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