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Bromine → 2-bromo-1-(2,3-dihydro-1H-inden-2-yl)ethan-1-one

HRID 1789388
ノート
印刷プレビュー

反応式

HRID 1789388 の反応式
[Br:1]Br.[CH2:3]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH2:5][CH:4]1[C:12](=[O:14])[CH3:13]>CCOCC>[Br:1][CH2:13][C:12]([CH:4]1[CH2:3][C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH2:5]1)=[O:14]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 24408Bromine3 回HCID 111163412-Acetylindane

生成物 1

HCID 153388302-bromo-1-(2,3-dihydro-1H-inden-2-yl)ethan-1-one

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

実験手順

Bromine (6.8 g) is slowly added to a stirred solution of 1-(2,3-dihydro-1H-inden-2-yl)ethanone (6.8 g) in 200 ml of dry ether, while keeping the temperature at +10° C. The rate of the addition of bromine is controlled so that the colour due to one added portion of bromine has been discharged before another portion is added. When the addition is complete, the ethereal solution is washed four times with 3M sodium carbonate solution, and is then washed three times with water. The ethereal solution is dried with anhydrous magnesium sulphate. After removal of the solvent the solid 2-bromo-1-(2,3-dihydro-1H-inden-2-yl)ethanone is obtained.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. customat +10° C
  2. additionis added
  3. additionWhen the addition
  4. washthe ethereal solution is washed four times with 3M sodium carbonate solution
  5. washis then washed three times with water
  6. dry with materialThe ethereal solution is dried with anhydrous magnesium sulphate
  7. customAfter removal of the solvent the solid 2-bromo-1-(2,3-dihydro-1H-inden-2-yl)ethanone
  8. customis obtained

出典と根拠

ORDレコード
ord-5c24f2117d6a447bb1c6127ce54bb126
出典データセット
uspto-grants-1987_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04689339

反応ノート

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