ChemicalBook > Product Catalog > Chemical Reagents > Organic reagents > Carboxylic anhydride > hexahydro-3,6-methanophthalic anhydride
hexahydro-3,6-methanophthalic anhydride
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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