反応 #45534

反応方程式

benzophenone

n-butyl lithium hexane

hexamethyl phosphoramide

hydrochloric acid

3-tert-butyl-cyclopentadiene

→

aimed compound

2-tert-butyl-6,6-diphenyl fulvene

溶媒

tetrahydrofuran

hexane

tetrahydrofuran

反応条件

後処理

1. 1
   その他In a 300 ml three-necked flask equipped with a magnetic stirrer
2. 2
   workup.STIRRINGfurther stirred at room temperature for 1 hr
3. 3
   その他To the solution, a solution prepared
4. 4
   workup.ADDITIONwas gradually added dropwise in an ice bath
5. 5
   workup.STIRRINGstirred at room temperature 1 day
6. 6
   workup.ADDITIONwas added
7. 7
   その他to separate an organic phase
8. 8
   洗浄The organic phase was washed with water and saturated brine
9. 9
   乾燥The organic phase was dried with anhydrous magnesium sulfate
10. 10
    ろ過the drying agent was filtered off
11. 11
    workup.DISTILLATIONthe solvent was distilled off from the filtrate under reduced pressure
12. 12
    その他to give dark-brown oil
13. 13
    その他The oil was purified with a column chromatography
14. 14
    workup.DISTILLATIONthe developing solvent was distilled off under reduced pressure

実験手順

In a 300 ml three-necked flask equipped with a magnetic stirrer and three-way cock was thoroughly purged with nitrogen, 4.75 g of 3-tert-butyl-cyclopentadiene (38.9 mmol) was dissolved in 100 ml of dehydrated tetrahydrofuran in a nitrogen atmosphere. To the solution, 26 ml of n-butyl lithium/hexane solution (1.58M: 41.1 mmol) was gradually added dropwise in an ice bath and stirred at room temperature over night. To the reaction solution, 21 ml of hexamethyl phosphoramide (121 mmol) dried with molecular sieves 4 A was added in the ice bath and further stirred at room temperature for 1 hr. To the solution, a solution prepared by dissolving 10.2 g of benzophenone (56.0 mmol) to 30 ml of dehydrated tetrahydrofuran was gradually added dropwise in an ice bath and stirred at room temperature 1 day. To the resulting reaction mixture, 100 ml of a hydrochloric acid aqueous solution (5%) was added. Thereafter, hexane was added to the mixed solution to separate an organic phase. The organic phase was washed with water and saturated brine. The organic phase was dried with anhydrous magnesium sulfate, thereafter the drying agent was filtered off and the solvent was distilled off from the filtrate under reduced pressure to give dark-brown oil. The oil was purified with a column chromatography using 400 g of silica gel (developing solvent: n-hexane) and the developing solvent was distilled off under reduced pressure, and thereby the aimed compound was obtained in an amount of 4.42 g (15.4 mmol) as an orange solid (yield: 40%).

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