反应 #1365722

ord-669f018a378e44c18b695fc3329d4d78

反应方程式

O
water
CC(Br)Br
dibromoethane
C1=Cc2ccccc2C1
indene
[Li][CH2]CCC
n-butyllithium
C1=CC(CCC2C=Cc3ccccc32)c2ccccc21
1.2-bisindenylethane
收率 51.6%

反应条件

温度
-78°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度to heat up to room temperature
  2. 2
    温度It was cooled to −78° C.
  3. 3
    workup.ADDITIONwere dropped (within 20 minutes)
  4. 4
    workup.ADDITIONAfter the end of the addition
  5. 5
    温度the temperature was raised to 50° C.
  6. 6
    workup.STIRRINGunder stirring for 12 hours
  7. 7
    温度was cooled down to room temperature
  8. 8
    其他The organic phase was dried
  9. 9
    萃取the residue was extracted with pentane
  10. 10
    其他By evaporation under vacuum 28.65 g of product
  11. 11
    其他were obtained (yield=51.6%)

实验过程

Into a 2 liter two-necked round-bottomed flask, 50 g of indene (437 mmol) were dissolved under inert atmosphere with 500 ml of tetrahydrofuran and were cooled to −78°C. By slow dropping (1 hour) 175 ml of n-butyllithium (2.5M in hexane, 437.5 mmol) were added. The mixture was allowed to heat up to room temperature and was kept under stirring for 4 hours. It was cooled to −78° C. and 40.42 g of dibromoethane (215 mmol) dissolved in 100 ml of tetrahydrofuran were dropped (within 20 minutes). After the end of the addition, the temperature was raised to 50° C., the whole was kept under stirring for 12 hours, then was cooled down to room temperature and 20 ml of water were added. The organic phase was dried and the residue was extracted with pentane. By evaporation under vacuum 28.65 g of product were obtained (yield=51.6%).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US06444604B1uspto-grants-2002_09