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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1415122생성일: 2026년 10월 27일

Ammonium Hydroxide → 4-[(3,6-Dichloropyridin-2-yl)methoxy]aniline

https://huagongshe.com/reaction/1415122

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium HydroxideHCID 14923—
반응물N-{4-[(3,6-Dichloropyridin-2-yl)methoxy]phenyl}acetamideHCID 20366210—
용매Boron, trifluoro(methanol)-, (T-4)-HCID 11062313—
생성물4-[(3,6-Dichloropyridin-2-yl)methoxy]anilineHCID 20366173—

반응 단계

N-(4-((3,6-Dichloro-2-pyridinyl)methoxy)phenyl)acetamide (30.27 grams; 0.097 mole) was mixed with a 270 ml. solution of boron trifluoride-methanol (1 gram per 10 ml.) and the resulting reaction mixture refluxed for a period of 4 1/2 hours. The reaction mixture was then diluted and cooled with ice water to a temperature of between about 0° to about 10° C. Concentrated ammonium hydroxide was added until the reaction mixture was basic. The reaction mixture was then extracted with portions of methylene chloride, the extracts combined and the solvent removed by evaporation. The residue thus obtained was extracted with five 500 ml. portions of hexane. The crystalline material which precipitated from the hexane mixture upon cooling was recovered by filtration. As a result of these operations, the desired 4-((3,6-dichloro-2-pyridinyl)methoxy)benzenamine compound was recovered as a light yellow crystalline solid having a melting point of 74°-75° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04003906
출처 데이터셋uspto-grants-1977_01
ORD IDord-ef8ea39bde8b463fa6fa7977bb5996ae
출처 메모uspto-grants-1977_01