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Potassium Iodide → (+/-)-Ethyl methyl 2,2'-(4-nitro-2,3-dihydro-1H-indole-1,3-diyl)diacetate

HRID 2353301
Notes
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Reaction equation

HRID 2353301 reaction equation
C[CH:2]([CH:6]1[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][C:13]=2[N+:15]([O-:17])=[O:16])[NH:8][CH2:7]1)[C:3]([O-:5])=[O:4].[C:18](=O)(O)[O-].[Na+].[I-].[K+].Br[CH2:26][C:27]([O:29][CH2:30][CH3:31])=[O:28]>CC(C)=O>[N+:15]([C:13]1[CH:12]=[CH:11][CH:10]=[C:9]2[C:14]=1[CH:6]([CH2:2][C:3]([O:5][CH3:18])=[O:4])[CH2:7][N:8]2[CH2:26][C:27]([O:29][CH2:30][CH3:31])=[O:28])([O-:17])=[O:16]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 4875Potassium IodideHCID 7748Ethyl bromoacetateHCID 516892Sodium BicarbonateHCID 66636769HCID 66636769, compound

Product 1

HCID 59257866(+/-)-Ethyl methyl 2,2'-(4-nitro-2,3-dihydro-1H-indole-1,3-diyl)diacetate

Reagents, catalysts & solvents 1

HCID 180
Acetone
Solvent

Procedure

To a solution of (±)-methyl(4-nitro-2,3-dihydro-1H-indol-3-yl)acetate from Step B (700 mg, 3.0 mmol), sodium bicarbonate (471 mg, 4.4 mmol), and potassium iodide (98 mg, 0.59 mmol) in acetone (15 mL) was added ethyl bromoacetate (9.9 mL, 88.9 mmol). The mixture was heated at reflux for 18 h, then cooled to ambient temperature and concentrated in vacuo. The residue was partitioned between H2O (15 mL) and EtOAc (2×40 mL) and the organic extracts were washed with brine, dried over Na2SO4, filtered, and concentrated in vacuo to a volume of 50 mL. Hexane was added to the EtOAc solution and a precipitate formed. The desired crystals were collected by vacuum filtration to give the title compound. MS: m/z 323 (M+1).

Workup

  1. temperatureThe mixture was heated
  2. temperatureat reflux for 18 h
  3. concentrationconcentrated in vacuo
  4. customThe residue was partitioned between H2O (15 mL) and EtOAc (2×40 mL)
  5. washthe organic extracts were washed with brine
  6. dry with materialdried over Na2SO4
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo to a volume of 50 mL
  9. additionHexane was added to the EtOAc solution
  10. customa precipitate formed
  11. filtrationThe desired crystals were collected by vacuum filtration

Sources & evidence

ORD record
ord-f2f152554ac74899a9d5399d5f4a1a0d
Source dataset
uspto-grants-2010_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07750010B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes