Ethyl bromoacetate → HCID 24823447, compound

HRID 1384961Notes

Reaction equation

HRID 1384961 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[C:9](=O)[NH:8][CH2:7][CH2:6]2.C[Si](C)(C)[N-][Si](C)(C)C.[K+].Br[CH2:25][C:26]([O:28][CH2:29][CH3:30])=[O:27]>C1COCC1>[CH2:29]([O:28][C:26](=[O:27])[CH2:25][N:8]1[CH2:7][CH2:6][C:5]2[C:10](=[CH:11][CH:12]=[C:3]([O:2][CH3:1])[CH:4]=2)[CH2:9]1)[CH3:30]

Participants

5

Conditions

Temperature
-78 °C

Procedure

To a solution of 3,4-dihydro-6-methoxy-l(2H)-isoquinolinone (852 mg, 4.81 mmol, prepared according to J. Chem. Soc., 1969, p 183) in THF (45 mL) at −78° C. was added 0.5M potassium hexamethyidisilazide (10.6 mL, 5.28 mmol) dropwise and the reaction mixture stirred at −78° C. for 5 minutes. The reaction mixture was warmed to 0° C. in a ice/water bath and ethyl bromoacetate (1.20 g, 7.21 mmol) was added dropwise and the mixture stirred at that temperature for 1 hour, and then at room temperature for 2 hours. The reaction mixture was quenched by addition of sat. NaHCO3, diluted with ethyl acetate, and the organic layer was washed with saturated NaHCO3 and then brine. It was dried (MgSO4) and concentrated in vacuo to afford the title compound (1.1 g, 86%) as a yellow solid. Molecular weight (MS): 263.

Workup

  1. temperatureThe reaction mixture was warmed to 0° C. in a ice/water bath
  2. stirringthe mixture stirred at that temperature for 1 hour
  3. waitat room temperature for 2 hours
  4. customThe reaction mixture was quenched by addition of sat. NaHCO3
  5. additiondiluted with ethyl acetate
  6. washthe organic layer was washed with saturated NaHCO3
  7. dry with materialIt was dried (MgSO4)
  8. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-3aa49c09af9844c29967e88abaa7a1d9
Source dataset
uspto-grants-2001_07
Patent number
US06262068B1

Reaction notes

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