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HRID 901701作成日:2026年10月25日

2-(4-Nitrophenoxy)naphthalene → 2-(4-Aminophenoxy)naphthalene

https://huagongshe.com/reaction/901701

反応式

関与物質

役割名称HCID仕込み量
反応物2-(4-Nitrophenoxy)naphthaleneHCID 762478—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
生成物2-(4-Aminophenoxy)naphthaleneHCID 3580829—

反応手順

The nitro intermediate (10 mmol) obtained above was dissolved in EtOH (50 mL) and hydrogenated in the presence of 10% Pd/C (300 mg) until completion according to General Procedure H, as indicated by TLC or HPLC. The reaction mixture was then filtered to remove the catalyst. The solvent was removed in vacuuo to afford the desired 4-(naphthalen-2-yloxy)aniline, which was used directly for further transformation without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07361678B2
出典データセットuspto-grants-2008_04
ORD IDord-4098d2e63ca645a590fc95b97a372b7b
出典メモuspto-grants-2008_04