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Carbon Dioxide → 7-Cyclopropylheptanoic acid

HRID 1730815
ノート
印刷プレビュー

反応式

HRID 1730815 の反応式
[Mg].BrCCBr.Br[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH:13]1[CH2:15][CH2:14]1.[C:16](=[O:18])=[O:17]>O1CCCC1>[CH:13]1([CH2:12][CH2:11][CH2:10][CH2:9][CH2:8][CH2:7][C:16]([OH:18])=[O:17])[CH2:15][CH2:14]1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 280Carbon DioxideHCID 78391,2-Dibromoethane2 回HCID 5462224MagnesiumHCID 22413033(6-Bromohexyl)cyclopropane

生成物 1

HCID 161141377-Cyclopropylheptanoic acid

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

0.684 g. Magnesium metal is covered with 2 ml. anhydrous tetrahydrofuran and 0.2 ml. 1,2-dibromoethane is added with stirring and heating. 1-Bromo-6-cyclopropylhexane (4.8 g.) and tetrahydrofuran (25 ml.) are added portionwise. An additional 0.207 ml. of 1,2-dibromethane is added and the reaction mixture refluxed for 3 hours. The solution is then maintained at 24°-28° while anhydrous carbon dioxide is bubbled through it for 11/2 hours. After stirring overnight under carbon dioxide, dry ether, water and 2N sulfuric acid are added until the pH is less than 7. The solution is extracted with ether and washed with water and brine, dried over calcium sulfate, filtered and the solvent removed to yield 7-cyclopropylheptanoic acid.

後処理

  1. temperatureheating
  2. temperaturethe reaction mixture refluxed for 3 hours
  3. customis bubbled through it for 11/2 hours
  4. stirringAfter stirring overnight under carbon dioxide
  5. additiondry ether, water and 2N sulfuric acid are added until the pH is less than 7
  6. extractionThe solution is extracted with ether
  7. washwashed with water and brine
  8. dry with materialdried over calcium sulfate
  9. filtrationfiltered
  10. customthe solvent removed

出典と根拠

ORDレコード
ord-c35bae9fc88043dd89c0afcbe366d5c9
出典データセット
uspto-grants-1976_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US03993773

反応ノート

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