Reaction equation
[CH3:1]I.N1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)CC1C(O)=O.[CH3:15][N:16]([CH3:19])[CH:17]=O.[C:20](=[O:23])([O-])[O-:21].[K+].[K+]>O>[CH3:15][N:16]1[C:19]2[C:11](=[CH:10][CH:9]=[CH:8][CH:7]=2)[CH2:6][CH:17]1[C:20]([O:21][CH3:1])=[O:23]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
11.7 ml of methyl iodide were added dropwise to a mixture of 10.3 g of (±)-indoline-2-carboxylic acid, 200 ml of dimethylformamide and 25.4 g of anhydrous potassium carbonate, and the resulting mixture was stirred at room temperature for 3 hours. At the end of this time, the reaction mixture was poured into water, after which it was extracted with ethyl acetate. The extract was washed with an aqueous solution of sodium chloride and dried over anhydrous sodium sulfate. The solvent was then removed by distillation under reduced pressure, and the resulting residue was purified by column chromatography through silica gel, using a 7:1 by volume mixture of hexane and ethyl acetate as the eluent, to give 9.12 g of the title compound having Rf=0.77 (on silica gel thin layer chromatography using a 2:1 by volume mixture of hexane and ethyl acetate as the developing solvent).
Workup
- extractionafter which it was extracted with ethyl acetate
- washThe extract was washed with an aqueous solution of sodium chloride
- dry with materialdried over anhydrous sodium sulfate
- customThe solvent was then removed by distillation under reduced pressure
- customthe resulting residue was purified by column chromatography through silica gel
- additionby volume mixture of hexane and ethyl acetate as the eluent
Sources & evidence
- ORD record
- ord-966454dd359340f6973c8bd716fa99f3
- Source dataset
- uspto-grants-1997_04
- Patent number
- US05624935
Linked notes
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