HRID328185

反应详情

EQUATION

反应方程式

HRID 328185 的结构方程式

PROCEDURE

实验过程

In a 50 ml. one-neck flask was placed 5.5 g. (0.0422 mol.) of 1,1-dimethoxy-3-methyl-2-butene and 10.0 g. (0.116 mol.) of prenol and 0.40 g. (0.002 mol.) of 2,4-dinitrophenol. The resulting solution was degassed with nitrogen and sealed with a serum cap and stirred at room temperature for 76 hours. The reaction solution was then diluted with 100 ml. of hexane and washed with 3 × 100 ml. of 1.0 N aqueous NaOH solution and 2 × 100 ml. of saturated aqueous NaCl solution. The combined water washings were back with extracted 1 × 50 ml. of hexane. The combined hexane solutions were dried (Na2SO4) and concentrated to give 9.0 g. of crude product. Distillation of 8.3 g. at 20 mmHg and a bath temperature of 55°-60° gave 1.48 g. of prenol. Continued distillation initially at 0.20 mmHg gave 2.43 g. of 1-methoxy-1-(3-methylbut-2-enoxy)-3-methyl-2-butene (b.p. 40°-45° at 0.20 mmHg) and finally at 0.050 mmHg gave 3.29 g. of 1,1-bis-(3-methylbut-2-enoxy)-3-methylbut-2-ene (b.p. 70°-75° at 0.050 mmHg).

WORKUP

后处理

  1. customone-neck flask was placed
  2. customThe resulting solution was degassed with nitrogen
  3. customsealed with a serum
  4. customcap
  5. additionThe reaction solution was then diluted with 100 ml
  6. washof hexane and washed with 3 × 100 ml
  7. extractionwith extracted 1 × 50 ml
  8. dry with materialThe combined hexane solutions were dried (Na2SO4)
  9. concentrationconcentrated
  10. customto give 9.0 g
  11. distillationDistillation of 8.3 g
  12. customat 20 mmHg and a bath temperature of 55°-60° gave 1.48 g
  13. distillationContinued distillation initially at 0.20 mmHg
  14. customgave 2.43 g