HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2114532Generated: October 27, 2026
Octahydro-1,4-methanonaphthalene → Exo-tricyclo[6.2.1.0(2.7)]undecane
https://huagongshe.com/reaction/2114532
Participants
| Role | Name | HCID | Charge |
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| Reactant | Octahydro-1,4-methanonaphthalene | HCID 13446694 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Exo-tricyclo[6.2.1.0(2.7)]undecane | HCID 549151 | 257.6% |
Reaction Steps
A 400 ml autoclave was charged with octahydro-1,4-methanonaphthalene (122 g, prepared as described above), methanol (100 ml, Burdick & Jackson, HPLC grade), and palladium on activated carbon (1.5 g containing 10% Pd, Alfa products, powder). The autoclave was closed and sealed, then shaken under 50 psig hydrogen pressure for 20 minutes at room temperature. The hydrogen pressure was increased to 200 psig for 10 minutes at room temperature followed by 600 psig at 70° C. for 45 minutes. Three identically prepared reaction mixtures were combined and filtered to remove the catalyst. The filtrate separated into two layers. The MeOH layer (top layer) was isolated and concentrated to give a residue, which was combined with product layer (the bottom layer). The combined crude product was distilled at reduced pressure to give decahydro-1,4-methanonaphthalene (318.6 g, bp 71-73° C./0.2 Torr, yield 86%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07435528B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-1f154975011342c0bdd1ee80b595c2b3 |
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| Source note | uspto-grants-2008_10 |
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