9-Phenylanthracene → 9-Bromo-10-phenyl-anthracene

HRID 546650

反応式

HRID 546650 の反応式
[C:1]1([C:7]2[C:8]3[C:13]([CH:14]=[C:15]4[C:20]=2[CH:19]=[CH:18][CH:17]=[CH:16]4)=[CH:12][CH:11]=[CH:10][CH:9]=3)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Br:21]Br.S([O-])([O-])(=O)=S.[Na+].[Na+]>C(Cl)(Cl)(Cl)Cl>[Br:21][C:14]1[C:15]2[C:20]([C:7]([C:1]3[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=3)=[C:8]3[C:13]=1[CH:12]=[CH:11][CH:10]=[CH:9]3)=[CH:19][CH:18]=[CH:17][CH:16]=2

参加物

5

実験手順

20.8 g (81.7 mmol) of 9-phenylanthracene and 300 mL of carbon tetrachloride were put into a 500 mL three-necked flask. A solution obtained by dissolving 13.1 g (81.7 mmol) of bromine in 5.00 mL of carbon tetrachloride was dropped into the mixture. After the dropping was completed, the reaction solution was stirred at room temperature for 3 hours to be reacted. Then, about 100 mL of a sodium thiosulfate solution was added to the reaction solution to complete the reaction. An organic layer of the mixture was washed with water and dried over magnesium sulfate. After the drying, the mixture was subjected to suction filtration, and the filtrate was condensed to obtain a solid. The obtained solid was recrystallized by a mixed solvent of chloroform and hexane; then 23.8 g of objective 9-bromo-10-phenylanthracene was obtained as a light yellow powdered solid in a yield of 71%. A synthetic scheme of 9-bromo-10-phenylanthracene is illustrated below (synthetic scheme b-2).

後処理

  1. customA solution obtained
  2. additionwas dropped into the mixture
  3. customto be reacted
  4. customthe reaction
  5. washAn organic layer of the mixture was washed with water
  6. dry with materialdried over magnesium sulfate
  7. filtrationAfter the drying, the mixture was subjected to suction filtration
  8. customcondensed
  9. customto obtain a solid
  10. customThe obtained solid was recrystallized by a mixed solvent of chloroform and hexane

出典と根拠

ORDレコード
ord-f9f67f0bbb5f49fcbd76d2eeafebd004
出典データセット
uspto-grants-2011_05
特許番号
US07935854B2

関連ノート

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