HRID1504243

反应详情

EQUATION

反应方程式

HRID 1504243 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
-78 °C

PROCEDURE

实验过程

3,3′-dibromo-5,5′-bis(trimethylsilyl)-2,2′-bithiophene (Compound E4, synthesized in accordance with WO 2010/136353, 11.4 g, 24.3 mmol) was placed in a 500 mL four-necked flask in a nitrogen atmosphere, and dissolved in tetrahydrofuran (200 mL). This was cooled to −78° C., and a solution of n-butyl lithium in hexane (KANTO CHEMICAL CO., INC., 1.59 M, 32.1 mL) was added dropwise. After about 20 minutes of agitation, the 3,7-dimethyloctyl-n-hexyl-dichlorosilane (Compound E24, 9.5 g) synthesized in Synthesis Example A22 was added dropwise. The temperature was raised gradually to room temperature over the course of about 2 hours, water was added, and the product was extracted with hexane. The organic layer was washed with water, and then dried over sodium sulfate and concentrated by filtration. The resulting oily substance was dissolved in chloroform (40 mL) and hexane (80 mL), trifluoroacetic acid (3.6 mL) was added, and the mixture was agitated for about 10 minutes at room temperature. Saturated sodium bicarbonate solution was added to the reaction solution, which was extracted with hexane and then concentrated under reduced pressure. The resulting yellow oily substance was dissolved in hexane, and subjected to silica gel column chromatography (solvent: hexane) to obtain the target 4-(3,7-dimethyloctyl)-4-n-hexyldithieno[3,2-b:2′,3′-d]silole (Compound E25, 8.2 g, yield 81%).

WORKUP

后处理

  1. additionwas added dropwise
  2. additionwas added
  3. extractionthe product was extracted with hexane
  4. washThe organic layer was washed with water
  5. dry with materialdried over sodium sulfate
  6. concentrationconcentrated by filtration
  7. dissolutionThe resulting oily substance was dissolved in chloroform (40 mL)
  8. additionhexane (80 mL), trifluoroacetic acid (3.6 mL) was added
  9. additionSaturated sodium bicarbonate solution was added to the reaction solution, which
  10. extractionwas extracted with hexane
  11. concentrationconcentrated under reduced pressure
  12. dissolutionThe resulting yellow oily substance was dissolved in hexane