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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2231787Generated: October 26, 2026

Acenaphthene → Acenaphthylene, dodecahydro-

https://huagongshe.com/reaction/2231787

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcenaphtheneHCID 6734—
CatalystRhodiumHCID 23948—
ProductAcenaphthylene, dodecahydro-HCID 102215100%

Reaction Steps

Acenaphthene was hydrogenated by the same procedure as in Example 4 except that the catalyst was replaced by a 5% Rh/C catalyst and reaction was effected at 150° C. for 30 minutes. Perhydroacenaphthene was produced in a yield of 100%, containing 1.1% of No. 1 isomer, 3.6% of No. 2 isomer, and 4.4% of No. 3 isomer, indicating a selectivity of No. 4 isomer of 90.9%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04783565
Source datasetuspto-grants-1988_11
ORD IDord-be6d29ca0ef3479797b3f28ae27053c0
Source noteuspto-grants-1988_11