Carbon Tetrachloride → HCID 12274172、化合物

HRID 355423ノート

反応式

HRID 355423 の反応式
[Br:1]N1C(=O)CCC1=O.[CH3:9][C:10]1[CH:23]=[CH:22][C:21]2[O:20][C:19]3[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=3)[C:13](=[O:24])[C:12]=2[CH:11]=1.C(Cl)(Cl)(Cl)Cl>C(OOC(=O)C1C=CC=CC=1)(=O)C1C=CC=CC=1.O>[Br:1][CH2:9][C:10]1[CH:23]=[CH:22][C:21]2[O:20][C:19]3[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=3)[C:13](=[O:24])[C:12]=2[CH:11]=1

参加物

6

反応物 3

HCID 5943Carbon TetrachlorideHCID 67184N-bromobutanimideHCID 2234732-Methylxanthen-9-one

生成物 1

HCID 12274172HCID 12274172、化合物収率 71.3%

試薬・触媒・溶媒 2

HCID 7187Benzoyl Peroxide触媒HCID 962Water溶媒

実験手順

Benzoyl peroxide (4.6 g, 19 mmol) and N-bromosuccinimide (67.6 g, 380 mmol) were added to a mixture of 2-methyl-9H-xanthen-9-one (79.9 g, 380 mmol) and carbon tetrachloride (800 ml) with heating under reflux, and the mixture was stirred for 4 hours. After spontaneous cooling to room temperature, water was added to the reaction mixture, and the reaction product was extracted with chloroform. The extract was washed with saturated sodium bicarbonate aqueous solution, water and saturated sodium chloride aqueous solution in that order, dried over anhydrous magnesium sulfate, and then concentrated under a reduced pressure. The resulting residue was recrystallized from ethyl acetate to give the title compound (78.3 g, 271 mmol, 71%) as yellow crystals.

後処理

  1. temperaturewith heating
  2. temperatureunder reflux
  3. extractionthe reaction product was extracted with chloroform
  4. washThe extract was washed with saturated sodium bicarbonate aqueous solution, water and saturated sodium chloride aqueous solution in that order
  5. dry with materialdried over anhydrous magnesium sulfate
  6. concentrationconcentrated under a reduced pressure
  7. customThe resulting residue was recrystallized from ethyl acetate

出典と根拠

ORDレコード
ord-3c3626e484a442759f6aeddab0aca5e9
出典データセット
uspto-grants-1998_11
特許番号
US05830902

反応ノート

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