反应 #45538

反应方程式

4,4′-dichloro-benzophenone

potassium hydroxide

hydrochloric acid

3-tert-butyl-1-methyl-cyclopentadiene

→

aimed compound

3-tert-butyl-1-methyl-6,6-di(4-chloro-phenyl)fulvene

溶剂

Diethyl ether

dimethoxy ethane

反应条件

后处理

1. 1
   其他In a 200 ml three-necked flask equipped with a magnetic stirrer chip and three-way cock
2. 2
   workup.ADDITIONwere added in a nitrogen atmosphere
3. 3
   温度under reflux for 3 days
4. 4
   workup.ADDITIONthe reaction mixture was gradually added dropwise
5. 5
   workup.STIRRINGstirred for some time
6. 6
   其他to separate an organic phase
7. 7
   洗涤The organic phase was washed with a saturated sodium bicarbonate aqueous solution, water and saturated brine
8. 8
   干燥The organic phase was dried with anhydrous magnesium sulfate
9. 9
   过滤the drying agent was filtered off
10. 10
    workup.DISTILLATIONthe solvent was distilled off from the filtrate under reduced pressure
11. 11
    其他to give a reddish-orange solid
12. 12
    其他The solid was purified with a column chromatography
13. 13
    workup.DISTILLATIONthe developing solvent was distilled off under reduced pressure

实验过程

In a 200 ml three-necked flask equipped with a magnetic stirrer chip and three-way cock thoroughly purged with nitrogen, 0.65 g of powdery potassium hydroxide (13.0 mmol) and 70 ml of dehydrated dimethoxy ethane were added in a nitrogen atmosphere. To the suspension, 1.24 g of 3-tert-butyl-1-methyl-cyclopentadiene (9.11 mmol) was added dropwise at room temperature and then 2.40 g of 4,4′-dichloro-benzophenone (9.58 mmol) was added and stirred under reflux for 3 days. To a 30 ml of a hydrochloric acid aqueous solution (1N) set in an ice bath, the reaction mixture was gradually added dropwise and stirred for some time. Diethyl ether was added to the mixed solution to separate an organic phase. The organic phase was washed with a saturated sodium bicarbonate aqueous solution, 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 a reddish-orange solid. The solid was purified with a column chromatography using 110 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 2.79 g (7.56 mmol) as a red solid (yield: 83%).

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