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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 21475생성일: 2026년 10월 24일

2-Fluoro-4-chloro-5-cyclopentyloxynitrobenzene → 4-Chloro-5-(cyclopentyloxy)-2-fluorobenzenamine

https://huagongshe.com/ko/reaction/21475

반응식

참여 물질

역할이름HCID투입량
반응물2-Fluoro-4-chloro-5-cyclopentyloxynitrobenzeneHCID 19374470—
촉매HCID 178418390HCID 178418390—
용매TolueneHCID 1140—
생성물4-Chloro-5-(cyclopentyloxy)-2-fluorobenzenamineHCID 15279389—

반응 단계

The resulting 2-fluoro-4-chloro-5-cyclopentyloxynitrobenzene (13.0 g, 50.1 mmol) was dissolved in toluene (100 ml), a catalytic amount of 10% palladium-carbon (0.5 g) was added thereto, and the mixture was reacted at room temperature to 70° C. under a hydrogen pressure of 3 to 5 atms. in a glass autoclave. After absorption of hydrogen gas ceased, the catalyst was removed by filtration, and the solvent was distilled off under reduced pressure from the filtrate to obtain substantially quantitatively oily 2-fluoro-4-chloro-5-cyclopentyloxyaniline. The spectral data and the like are as described in Reference Example 1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05424277
출처 데이터셋uspto-grants-1995_06
ORD IDord-67f78207c5b64f1ab0a8cb7a7aad0bee
출처 메모uspto-grants-1995_06