Реакция #1027

ord-1933fe9b9be74b32bfee65861da57c2d

Уравнение реакции

[CH3][Mg][Cl]
Methyl magnesium chloride
N#Cc1cc2ccccc2cn1
isoquinoline-3-carbonitrile
C1CCOC1
THF
CC(=O)c1cc2ccccc2cn1
3-acetyl-isoquinoline
Выход 14.0%

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.ADDITIONAfter the addition the reaction mixture
  2. 2
    Другоеquenched with water
  3. 3
    workup.ADDITIONHydrochloric acid (2M aqueous solution) was added to the reaction mixture until the aqueous phase
  4. 4
    workup.STIRRINGAfter stirring for 30 minutes the
  5. 5
    Экстракцияextracted with ether (×2)
  6. 6
    ПромывкаThe combined extracts were washed with water
  7. 7
    Другоеdried
  8. 8
    Концентрированиеconcentrated
  9. 9
    Другоеto give a crystalline solid
  10. 10
    ДругоеRecrystalisation from hexane

Методика

Methyl magnesium chloride (2.6 ml of a 3.0M solution in THF) was added dropwise to a solution of isoquinoline-3-carbonitrile at 0°-5° C. After the addition the reaction mixture was stirred at room temperature for 1 hour, then quenched with water. Hydrochloric acid (2M aqueous solution) was added to the reaction mixture until the aqueous phase was pH2. After stirring for 30 minutes the aqueous was neutralised with sodium bicarbonate (solid) and extracted with ether (×2). The combined extracts were washed with water, dried and concentrated to give a crystalline solid. Recrystalisation from hexane gave 3-acetyl-isoquinoline (0.55 g, 14% yield) as a pale yellow solid m.p. 84.4°-86.8° C. 1H NMR: 2.83(3H,s); 7.69-7.81(2H,m); 7.99(1H,m); 8.04(1H,m); 8.49(1H,m); 9.29(1H,s) ppm.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05723473uspto-grants-1998_03