Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2114533Generated: October 30, 2026

HCID 22020358, compound → Decahydro-2-trifluoromethyl-1,4-methanonaphthalene

https://huagongshe.com/reaction/2114533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22020358HCID 22020358—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductDecahydro-2-trifluoromethyl-1,4-methanonaphthaleneHCID 22020359—

Reaction Steps

A 400 ml autoclave is charged with 177 g of the thus purified octahydro-2-trifluormethyl-1,4-methanonaphthalene, methanol (100 ml, Burdick & Jackson, HPLC grade), and palladium on activated carbon (1.5 g containing 10% Pd, Alfa products, powder). The autoclave is closed and sealed, then it is shaken under 50 psig hydrogen pressure for 20 minutes at room temperature. The hydrogen pressure is increased to 200 psig for 10 minutes at room temperature followed by 600 psig at 70° C. for 45 minutes. The decahydro-2-trifluormethyl-1,4-methanonaphthalene product is purified by distillation at reduced pressure. The distilled product is then treated with concentrated sulfuric acid followed by silica gel treatment similar to what described in the example 2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07435528B2
Source datasetuspto-grants-2008_10
ORD IDord-d1ca5809758445d1aedb96a331d6261a
Source noteuspto-grants-2008_10