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HRID 34480作成日:2026年10月26日

Acenaphthene → Acenaphthylene, dodecahydro-

https://huagongshe.com/reaction/34480

反応式

関与物質

役割名称HCID仕込み量
反応物AcenaphtheneHCID 6734—
触媒NickelHCID 935—
生成物Acenaphthylene, dodecahydro-HCID 102215100%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04761510
出典データセットuspto-grants-1988_08
ORD IDord-4c6ddff5b3c744a1827fabacb7509121
出典メモuspto-grants-1988_08