反応 #717767

反応方程式

sodium cyclopentadienide

n-nonanophenone

→

6-(n-octyl)-6-phenylfulvene

収率 72.5%

溶媒

THF

THF

反応条件

後処理

1. 1
   その他to produce a solution
2. 2
   温度under cooling with ice
3. 3
   その他Then, the obtained deep red solution was quenched with dilute aqueous hydrochloric acid
4. 4
   温度under cooling with ice
5. 5
   workup.ADDITIONThen, 30 mL of diethyl ether was added
6. 6
   抽出the soluble part in diethyl ether was extracted
7. 7
   洗浄washed with an aqueous solution of saturated sodium hydrogen carbonate, water
8. 8
   workup.DISTILLATIONThe solvent was distilled off
9. 9
   その他the residue was purified by silica gel column chromatography
10. 10
    その他to obtain an objective that

実験手順

Under a nitrogen atmosphere, 2.0 g (9.2 mmol) of n-nonanophenone and 30 mL of dry THF were put into a 100-mL Schlenk flask to produce a solution. To this solution, 5.6 mL (11.2 mmol) of a solution of 2.0-M sodium cyclopentadienide in THF was added under cooling with ice, and the product was stirred at room temperature for 19 hours. Then, the obtained deep red solution was quenched with dilute aqueous hydrochloric acid under cooling with ice. Then, 30 mL of diethyl ether was added thereto, and the soluble part in diethyl ether was extracted, and the organic layer was neutralized and washed with an aqueous solution of saturated sodium hydrogen carbonate, water, and a saturated salt solution and then dehydrated with anhydrous magnesium sulfate. The solvent was distilled off, and then the residue was purified by silica gel column chromatography to obtain an objective that was a red liquid (amount: 1.77 g and yield: 72.5%).

出典