反应 #358201

反应方程式

chlorotrimethylsilane

1-(cyclopentadienyl)-1-(1,1,4,4,7,7,10,10-octamethyl-1,2,3,4,7,8,9,10-octahydrodibenzo(b,h)-fluorenyl)diphenylmethane

hexane

n-BuLi

→

light yellow amorphous product

收率 61.0%

1-(3-trimethylsilylcyclopentadienyl)-1-(1,1,4,4,7,7,10,10-octamethyl-1,2,3,4,7,8,9,10-octahydrodibenzo(b,h)-fluorenyl)diphenylmethane

收率 61.0%

溶剂

THF

反应条件

后处理

1. 1
   其他was placed at room temperature
2. 2
   其他to give a solution
3. 3
   温度The solution was cooled with an ice bath (light orangy brown solution)
4. 4
   其他Then, the ice bath was removed
5. 5
   workup.STIRRINGthe solution was stirred at room temperature for 18 hours (dark red solution)
6. 6
   温度The solution was cooled with an ice bath
7. 7
   其他The ice bath was removed
8. 8
   workup.STIRRINGthe solution was stirred at room temperature for 3 hours
9. 9
   workup.ADDITIONThe resulting dark brown solution was poured into 50 ml of a diluted hydrochloric acid solution
10. 10
    其他to perform quenching
11. 11
    萃取After the soluble component was extracted with 30 ml of diethyl ether
12. 12
    洗涤the organic phase was washed with 50 ml of a saturated saline solution
13. 13
    干燥The organic phase was dried over MgSO4
14. 14
    过滤the MgSO4 was filtered off
15. 15
    workup.DISTILLATIONdistilled off by a rotary evaporator
16. 16
    其他to obtain a yellowish brown amorphous product
17. 17
    其他The amorphous product was purified by silica gel column chromatography (developing solvent: hexane:dichloromethane=19:1)

实验过程

In a 30 ml Schlenk flask purged with nitrogen, 0.92 g (1.48 mmol, 1 eq) of 1-(cyclopentadienyl)-1-(1,1,4,4,7,7,10,10-octamethyl-1,2,3,4,7,8,9,10-octahydrodibenzo(b,h)-fluorenyl)diphenylmethane was placed at room temperature. Then, 20 ml of dehydrated THF was added, and the mixture was stirred by a magnetic stirrer to give a solution. The solution was cooled with an ice bath (light orangy brown solution). To the solution, 1.0 ml (1.63 mmol, 1.10 eq) of a hexane solution of n-BuLi was dropwise added. Then, the ice bath was removed, and the solution was stirred at room temperature for 18 hours (dark red solution). The solution was cooled with an ice bath, and to the solution, 1.05 ml (8.28 mmol, 5.59 eq) of chlorotrimethylsilane was dropwise added by a syringe (dark brown solution). The ice bath was removed, and the solution was stirred at room temperature for 3 hours. The resulting dark brown solution was poured into 50 ml of a diluted hydrochloric acid solution to perform quenching. After the soluble component was extracted with 30 ml of diethyl ether, the organic phase was washed with 50 ml of a saturated saline solution. The organic phase was dried over MgSO4, then the MgSO4 was filtered off, and from the filtrate the solvent was vacuum distilled off by a rotary evaporator to obtain a yellowish brown amorphous product. The amorphous product was purified by silica gel column chromatography (developing solvent: hexane:dichloromethane=19:1) to obtain 0.62 g a light yellow amorphous product (yield: 61%)

来源