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Hydrogen Bromide → 1,3-Bis(3,5-dibromophenyl)adamantane

HRID 7221
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HRID 7221 반응식
Br[C:2]12[CH2:11][CH:6]3[CH2:7][CH:8]([CH2:10][C:4](Br)([CH2:5]3)[CH2:3]1)[CH2:9]2.[Br-:13].[Al+3].[Br-:15].[Br-].[Br:17][C:18]1[CH:23]=[CH:22][CH:21]=[C:20]([Br:24])[CH:19]=1.Br>>[Br:17][C:18]1[CH:23]=[C:22]([C:2]23[CH2:11][CH:6]4[CH2:7][CH:8]([CH2:10][C:4]([C:2]5[CH:11]=[C:6]([Br:13])[CH:5]=[C:4]([Br:15])[CH:3]=5)([CH2:5]4)[CH2:3]2)[CH2:9]3)[CH:21]=[C:20]([Br:24])[CH:19]=1
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참가 물질

5

반응물 4

HCID 260Hydrogen BromideHCID 79271,3-DibromobenzeneHCID 166749BromhydrolHCID 2657901,3-Dibromoadamantane

생성물 1

HCID 220202971,3-Bis(3,5-dibromophenyl)adamantane수율 194.3%

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온도
0 °C

실험 절차

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.

후처리

  1. customAfter the air inside a 1 litter flask equipped with a thermometer and stirrer
  2. temperaturewas cooled to 5° C. in advance
  3. customreacted at an inside temperature of 0 to 10° C. for 7 hours
  4. customwas absorbed into an aqueous alkaline solution for the removal of its toxicity
  5. customAfter the completion of the reaction, 130 g of 4% by weight hydrochloric acid
  6. additionwas slowly dropped
  7. stirringthe solution was stirred until the orange color of the reaction solution
  8. customseparated by funnel
  9. washThe resulting organic phase was washed with water three times
  10. addition190 grams of toluene was added to the organic phase after the washing, which
  11. temperaturewas then warmed
  12. customto remove water
  13. temperatureunder reflux
  14. temperatureThen, the organic solution was cooled
  15. filtrationthe crystal deposited was collected by filtration
  16. washto washing with toluene, methanol and water
  17. customby drying under reduced pressure

출처 및 근거

ORD 기록
ord-056f03b2844a43409ccd9457a545328f
출처 데이터셋
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07084287B2

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