Sodium Carbonate → 5-bromo-3,3-dimethyl-2,3-dihydro-1H-indol-2-one

HRID 1760298Notes

Reaction equation

HRID 1760298 reaction equation
[CH3:1][C:2]1([CH3:12])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[NH:4][C:3]1=[O:11].C([O-])(=O)C.[Na+].[Br:18]Br.C(=O)([O-])[O-].[Na+].[Na+]>C(O)(=O)C.O>[Br:18][C:8]1[CH:9]=[C:10]2[C:5](=[CH:6][CH:7]=1)[NH:4][C:3](=[O:11])[C:2]2([CH3:12])[CH3:1]

Participants

7

Reactant 4

HCID 10340Sodium CarbonateHCID 24408BromineHCID 3131003,3-Dimethyl-1,3-dihydro-indol-2-oneHCID 517045Sodium Acetate

Product 1

HCID 120527965-bromo-3,3-dimethyl-2,3-dihydro-1H-indol-2-oneYield 92%

Reagents, catalysts & solvents 2

HCID 176Acetic AcidSolvent2×HCID 962WaterSolvent

Procedure

3,3-dimethyl-indol-2-one (0.65 g, 4.03 mmol) and sodium acetate (0.33 g, 4.07 mmol) were stirred in acetic acid (5 cm3) then bromine (0.66 g, 4.13 mmol) in acetic acid (5 cm3) was added drop-wise to the reaction mixture. The reaction was stirred for 50 min., then poured into water. The mixture was basified with sodium carbonate, extracted with ethyl acetate (×3), dried (MgSO4), filtered, and evaporated to give the subtitled compound (0.89 g, 92%) 1H NMR (DMSO-d6) δ 1.21 (s, 6 H), 6.76 (d, 1 H, J=8.22 Hz), 7.29 (dd, 1 H, J=2.12 Hz, 8.23 Hz), 7.49 (d, 1 H, J=2.03 Hz), 10.4 (s, 1H).

Workup

  1. extractionextracted with ethyl acetate (×3)
  2. dry with materialdried (MgSO4)
  3. filtrationfiltered
  4. customevaporated

Sources & evidence

ORD record
ord-c05ddd28120240e8a0eca607a6b03921
Source dataset
uspto-grants-2005_01
Patent number
US06841568B2

Reaction notes

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