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Sulfuric Acid → 2,3-Norbornanedicarboxylic acid

HRID 1359187
ノート
印刷プレビュー

反応式

HRID 1359187 の反応式
[CH:1]12[CH2:7][CH:4]([CH2:5][CH2:6]1)[CH:3]([C:8]([O-:10])=[O:9])[CH:2]2[C:11]([O-:13])=[O:12].[Na+].[Na+].S(=O)(=O)(O)O>O>[CH:1]12[CH2:7][CH:4]([CH2:5][CH2:6]1)[CH:3]([C:8]([OH:10])=[O:9])[CH:2]2[C:11]([OH:13])=[O:12]
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 1118Sulfuric AcidHCID 21981355bicyclo2.2.1heptane-2,3-dicarboxylic acid, disodium salt

生成物 1

HCID 998352,3-Norbornanedicarboxylic acid

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

100.0 g (438.3 mmoles) of disodium bicyclo[2.2.1]heptane-2,3-dicarboxylate (228.15 g/mole) and 280 ml of water were charged into a 2L Erlenmeyer flask with stirring. To this solution was added fuming sulfuric acid until the pH of the resulting solution was ˜1. As the pH became acidic, a white flocculent precipitate formed. The solution was stirred and cooled to room temperature. The precipitate was removed by vacuum filtration and dried overnight in a vacuum oven at 110° C. The resulting product (melting point of 152.1-153.4° C.) was dried and milled. An IR analysis was consistent with that of the expected structure.

後処理

  1. additionTo this solution was added
  2. customa white flocculent precipitate formed
  3. stirringThe solution was stirred
  4. customThe precipitate was removed by vacuum filtration
  5. customdried overnight in a vacuum oven at 110° C
  6. dry with materialThe resulting product (melting point of 152.1-153.4° C.) was dried
  7. custommilled

出典と根拠

ORDレコード
ord-a3d9a6992c184dfea2864462bfdcda9b
出典データセット
uspto-grants-2003_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06599968B2

反応ノート

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