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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 901701생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/901701

반응식

참여 물질

역할이름HCID투입량
반응물2-(4-Nitrophenoxy)naphthaleneHCID 762478—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
생성물2-(4-Aminophenoxy)naphthaleneHCID 3580829—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07361678B2
출처 데이터셋uspto-grants-2008_04
ORD IDord-4098d2e63ca645a590fc95b97a372b7b
출처 메모uspto-grants-2008_04