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Sulfuric Acid → 2,3-Norbornanedicarboxylic acid

HRID 1359187
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1359187
[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]
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Komponenten

4

Edukt 2

HCID 1118Sulfuric AcidHCID 21981355bicyclo2.2.1heptane-2,3-dicarboxylic acid, disodium salt

Produkt 1

HCID 998352,3-Norbornanedicarboxylic acid

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

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.

Aufarbeitung

  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

Quellen und Nachweise

ORD-Eintrag
ord-a3d9a6992c184dfea2864462bfdcda9b
Quelldatensatz
uspto-grants-2003_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06599968B2

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