反应 #7317

反应方程式

hydrogen bromide

1,3-dibromoadamantane

aluminum bromide

1,3-dibromobenzene

→

1,3-bis(3,5-dibromophenyl)adamantane

收率 194.3%

反应条件

后处理

1. 1
   其他After the air inside a 1 litter flask equipped with a thermometer and stirrer
2. 2
   温度was cooled to 5° C. in advance
3. 3
   其他reacted at an inside temperature of 0 to 10° C. for 7 hours
4. 4
   其他was absorbed into an aqueous alkaline solution for the removal of its toxicity
5. 5
   其他After the completion of the reaction, 130 g of 4% by weight hydrochloric acid
6. 6
   workup.ADDITIONwas slowly dropped
7. 7
   workup.STIRRINGthe solution was stirred until the orange color of the reaction solution
8. 8
   其他separated by funnel
9. 9
   洗涤The resulting organic phase was washed with water three times
10. 10
    workup.ADDITION190 grams of toluene was added to the organic phase after the washing, which
11. 11
    温度was then warmed
12. 12
    其他to remove water
13. 13
    温度under reflux
14. 14
    温度Then, the organic solution was cooled
15. 15
    过滤the crystal deposited was collected by filtration
16. 16
    洗涤to washing with toluene, methanol and water
17. 17
    其他by drying under reduced pressure

实验过程

After the air inside a 1 litter flask equipped with a thermometer and stirrer was replaced by nitrogen, 43 g of 1,3-dibromoadamantane and 10 g of anhydrous aluminum bromide were placed therein, and then the inside of the flask was cooled to 0° C. Thereto was added 190 g of 1,3-dibromobenzene that was cooled to 5° C. in advance, and the resulting material was agitated and reacted at an inside temperature of 0 to 10° C. for 7 hours. The reaction was carried out while the hydrogen bromide gas that was generated during the reaction was absorbed into an aqueous alkaline solution for the removal of its toxicity. After the completion of the reaction, 130 g of 4% by weight hydrochloric acid was slowly dropped and then the solution was stirred until the orange color of the reaction solution faded away. The agitation was stopped and the resulting solution was allowed to stand and then separated by funnel. The resulting organic phase was washed with water three times. 190 grams of toluene was added to the organic phase after the washing, which was then warmed to remove water under reflux. Then, the organic solution was cooled and the crystal deposited was collected by filtration. The resulting crystal was subjected to washing with toluene, methanol and water, followed by drying under reduced pressure to obtain 44 g of 1,3-bis(3,5-dibromophenyl)adamantane.

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