Formic Acid → N-Formylindoline
Reaction equation
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][CH2:2]1.[CH:10](O)=[O:11]>C1(C)C=CC=CC=1>[CH:10]([N:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][CH2:2]1)=[O:11]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of indoline (5.0 g) and 98% formic acid (3.0 g) in toluene (17 mL) was heated at reflux for 6 hours with a Dean-Stark trap, cooled, washed with water and concentrated. The resulting dark brown solid was dissolved in methanol, concentrated to a fraction of its original volume, treated with 1:1 diethyl ether/hexane, and concentrated dryness to provide 5.5 g of the desired product.
Workup
- temperatureat reflux for 6 hours with a Dean-Stark trap
- temperaturecooled
- washwashed with water
- concentrationconcentrated
- dissolutionThe resulting dark brown solid was dissolved in methanol
- concentrationconcentrated to a fraction of its original volume
- additiontreated with 1:1 diethyl ether/hexane
- concentrationconcentrated dryness
Sources & evidence
- ORD record
- ord-8ba5063601094e65bdede409e8352da1
- Source dataset
- uspto-grants-2003_02
- Patent number
- US06521658B1
Reaction notes
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