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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 74183생성일: 2026년 10월 23일

Acetic Acid → 5-Bromo-2-(tetrahydropyran-4-yl)aminoaniline

https://huagongshe.com/ko/reaction/74183

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물5-Bromo-2-(tetrahydropyran-4-yl)nitrobenzeneHCID 67498826—
촉매IronHCID 23925—
생성물5-Bromo-2-(tetrahydropyran-4-yl)aminoanilineHCID 4360981485.4%

반응 단계

A 3-neck flask was charged with 5-bromo-2-(tetrahydropyran-4-yl)nitrobenzene (see Working Example 18-1) (3.54 g, 11.8 mmol) and 10% aqueous acetic acid solution (65 mL), after which electrolytic iron (6.56 g, 118 mmol) was added and this was refluxed with stirring for 15 minutes. After this was allowed to cool to room temperature, the insoluble material was filtered off through Celite, and this same layer was further washed with 10% aqueous acetic acid solution (65 mL). The filtrate and the wash solutions were combined and then successively extracted with ethyl acetate (approx. 50 mL, 4 times), washed with distilled water (30 mL), and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and further drying under reduced pressure yielded the title compound (2.72 g, 85.4% yield) as a pale yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829035B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-6d53bc48aa9b474c99fc67ba238410a5
출처 메모uspto-grants-2014_09