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

HRID 1789388
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HRID 1789388 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24408Bromine3회HCID 111163412-Acetylindane

생성물 1

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

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

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.

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후처리

  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

출처 및 근거

ORD 기록
ord-5c24f2117d6a447bb1c6127ce54bb126
출처 데이터셋
uspto-grants-1987_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04689339

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