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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1995839생성일: 2026년 10월 25일

5-[(4-Chlorophenyl)methoxy]-2-nitropyridine → 5-[(4-Chlorophenyl)methoxy]pyridin-2-amine

https://huagongshe.com/reaction/1995839

반응식

참여 물질

역할이름HCID투입량
반응물5-[(4-Chlorophenyl)methoxy]-2-nitropyridineHCID 20486129—
촉매WaterHCID 962—
용매MethanolHCID 887—
생성물5-[(4-Chlorophenyl)methoxy]pyridin-2-amineHCID 20486112—

반응 단계

A mixture of 5-(4-chlorobenzyloxy)-2-nitropyridine (0.5 g), Na2S (0.25 g) and methanol (12 ml) is heated to reflux for about 3 hours. Then, a few drops of water is added and refluxing continued about 15 hours. After cooling, the reaction is diluted with methanol, filtered through celite and stripped. The concentrate is taken up in CHCl3, washed with water, dried and stripped giving 2-amino-5-(4-chlorobenzyloxy)pyridine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04406689
출처 데이터셋uspto-grants-1983_09
ORD IDord-d0b88793ae6c414990b04c5246241a74
출처 메모uspto-grants-1983_09