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hexahydro-3,6-methanophthalic anhydride

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hexahydro-3,6-methanophthalic anhydride Basic information

Product Name:
hexahydro-3,6-methanophthalic anhydride
Synonyms:
  • hexahydro-3,6-methanophthalic anhydride
  • 3a,4,5,6,7,7a-Hexahydro-4,7-methanoisobenzofuran-1,3-dione
  • 4-Oxatricyclo[5.2.1.02,6]decane-3,5-dione
  • Bicyclo[2.2.1]heptane-2,3-dicarboxylic anhydride
  • Einecs 227-852-8
  • Hexahydro-4,7-Methanoisobenzofuran-1,3-dione
  • 4,7-Methanoisobenzofuran-1,3-dione, hexahydro-
CAS:
6004-79-1
MF:
C9H10O3
MW:
166.17
EINECS:
227-852-8
Mol File:
6004-79-1.mol
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hexahydro-3,6-methanophthalic anhydride Chemical Properties

Boiling point:
325.2±11.0 °C(Predicted)
Density 
1.345
InChI
InChI=1S/C9H10O3/c10-8-6-4-1-2-5(3-4)7(6)9(11)12-8/h4-7H,1-3H2
InChIKey
LQOPXMZSGSTGMF-UHFFFAOYSA-N
SMILES
C1(=O)C2C(C3CC2CC3)C(=O)O1
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hexahydro-3,6-methanophthalic anhydride Usage And Synthesis

Synthesis

The production method uses maleic anhydride and mixed C5s as raw materials, generates Nadic anhydride by absorbing cyclopentadiene with maleic anhydride directly at a temperature of 0-5°C, and crystallizes to obtain a pure product; and a Cu-Ni/ZnO-ZrO2 or Co-Ni/ZnO-ZrO2 catalyst is added to the generated Nadic anhydride, carrying out a catalytic hydrogenation reaction in a high-pressure autoclave for 4-6 hours at a temperature of 100-140°C and under a hydrogen pressure of 1-4 MPa, the catalyst is filtered after cooling, and reduced pressure distilling to obtain the hexahydro-3,6-methanophthalic anhydride.[1]

References

[1] Endo-methylene hexahydrophthalic anhydride and production method thereof. Patent EP2495241A1.

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