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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34480Generated: October 26, 2026

Acenaphthene → Acenaphthylene, dodecahydro-

https://huagongshe.com/reaction/34480

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcenaphtheneHCID 6734—
CatalystNickelHCID 935—
ProductAcenaphthylene, dodecahydro-HCID 102215100%

Reaction Steps

Acenaphthene was hydrogenated by the same procedure as in Example 1 except that the catalyst was replaced by a Raney nickel catalyst. Perhydroacenaphthene was produced in a yield of 100%, but the yields of Nos. 1 to 4 isomers were 18.9%, 8.3%, 37.4%, and 35.4%, respectively.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04761510
Source datasetuspto-grants-1988_08
ORD IDord-4c6ddff5b3c744a1827fabacb7509121
Source noteuspto-grants-1988_08