反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
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
- additionwas added dropwise
- additionwas added
- extractionthe product was extracted with hexane
- washThe organic layer was washed with water
- dry with materialdried over sodium sulfate
- concentrationconcentrated by filtration
- dissolutionThe resulting oily substance was dissolved in chloroform (40 mL)
- additionhexane (80 mL), trifluoroacetic acid (3.6 mL) was added
- additionSaturated sodium bicarbonate solution was added to the reaction solution, which
- extractionwas extracted with hexane
- concentrationconcentrated under reduced pressure
- dissolutionThe resulting yellow oily substance was dissolved in hexane