HRID61335

反应详情

EQUATION

反应方程式

HRID 61335 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
30 °C

PROCEDURE

实验过程

Methyl lithium in tetrahydrofuran (THF) (1.6 L, 1 M) was charged to a flame dried 3 L reaction flask equipped with a thermometer, a mechanical stirrer, condenser, and an addition funnel. Citral was added dropwise for over 2-2.5 hours. The reaction mixture was aged until the conversion rate was greater than 90%. The reaction mixture was cooled to lower than 30° C. and quenched by the slow addition of HCl (pH<5.10%). The aqueous phase was extracted three times with toluene (100 mL) and the extracts were added to the crude reaction mixture. The crude reaction mixture was then washed with saturated sodium bicarbonate (500 mL) followed by saturated salt solution and dried over anhydrous sodium sulphate. The crude reaction mixture was concentrated. The solvents were recovered via a rotary evaporator to provide 8-hydroxy-2,6-dimethyl-nona-2,6-diene.

WORKUP

后处理

  1. customdried
  2. custom3 L reaction flask
  3. customequipped with a thermometer, a mechanical stirrer, condenser, and an addition funnel
  4. customquenched by the slow addition of HCl (pH<5.10%)
  5. extractionThe aqueous phase was extracted three times with toluene (100 mL)
  6. additionthe extracts were added to the crude
  7. customreaction mixture
  8. customThe crude reaction mixture
  9. washwas then washed with saturated sodium bicarbonate (500 mL)
  10. dry with materialdried over anhydrous sodium sulphate
  11. customThe crude reaction mixture
  12. concentrationwas concentrated
  13. customThe solvents were recovered via a rotary evaporator