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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOctahydro-1,4-methanonaphthaleneHCID 13446694—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductExo-tricyclo[6.2.1.0(2.7)]undecaneHCID 549151257.6%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07435528B2
Source datasetuspto-grants-2008_10
ORD IDord-1f154975011342c0bdd1ee80b595c2b3
Source noteuspto-grants-2008_10