Potassium Carbonate → Ethyl 2-(hydroxyimino)-3-(4,6-dichloro-3-indolyl)propanoate
Reaction equation
[Cl:1][C:2]1[CH:10]=[C:9]([Cl:11])[CH:8]=[C:7]2[C:3]=1[CH:4]=[CH:5][NH:6]2.C(=O)([O-])[O-].[K+].[K+].Br[CH2:19][C:20](=[N:26][OH:27])[C:21]([O:23][CH2:24][CH3:25])=[O:22]>C(Cl)Cl>[OH:27][N:26]=[C:20]([CH2:19][C:4]1[C:3]2[C:7](=[CH:8][C:9]([Cl:11])=[CH:10][C:2]=2[Cl:1])[NH:6][CH:5]=1)[C:21]([O:23][CH2:24][CH3:25])=[O:22]Participants
Procedure
Mix 4,6-dichloroindole (5.90 g, 31.72 mmol), potassium carbonate (1.81 g, 47.6 mmol) and anhydrous methylene chloride (200 mL). Stir and add a solution of ethyl 3-bromo-2-hydroxyiminopropanoate (7.00 g, 33.31 mmol) in methylene chloride (75 mL). Stir under a nitrogen atmosphere for 48 hours. Take the solution up in methylene chloride (100 mL) and wash with water (300 mL), saturated sodium hydrogen carbonate (200 mL) and brine (100 mL). Dry (MgSO4) and evaporate the solvent in vacuo to give a tan solid. Purify by silica gel chromatography (1 to 3% acetone in chloroform) to give the title compound as a yellow solid (7.00 g, 99% based on consumed starting material). Recrystallize (diethyl ether/hexane) to give the title compound as white crystals (4.0 g, 56%); mp 175°-176° C.
Workup
- stirringStir under a nitrogen atmosphere for 48 hours
- washwash with water (300 mL), saturated sodium hydrogen carbonate (200 mL) and brine (100 mL)
- dry with materialDry (MgSO4)
- customevaporate the solvent in vacuo
- customto give a tan solid
- customPurify by silica gel chromatography (1 to 3% acetone in chloroform)
Sources & evidence
- ORD record
- ord-152055314a71431d997e2bdbabd64285
- Source dataset
- uspto-grants-1995_11
- Patent number
- US05470870
Reaction notes
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