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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 222028생성일: 2026년 10월 25일

Ethyl Acetate → 3-Chloro-4-(2-pyridylmethoxy)aniline

https://huagongshe.com/reaction/222028

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물2-((2-Chloro-4-nitrophenoxy)methyl)pyridineHCID 17469433—
촉매IronHCID 23925—
용매Acetic AcidHCID 176—
생성물3-Chloro-4-(2-pyridylmethoxy)anilineHCID 1678121252%

반응 단계

2-(2-chloro-4-nitro-phenoxymethyl)-pyridine (8 g, 30.2 mmol, 1 equiv) and 8.44 g iron (151.1 mmol, 5 equiv) were mixed in 100 mL acetic acid and 50 mL EtOAc and were stirred at rt overnight. The reaction mixture was filtered through a pad of Celite®. The filtrate was concentrated in vacuo and neutralized with saturated Na2CO3 solution. The solution was extracted with EtOAc and the organic layer was washed with brine and concentrated in vacuo. The resulting crude material was purified by flash chromatography eluting with EtOAc/hexane (3:7) to give 3-Chloro-4-(pyridin-2-ylmethoxy)-phenylamine (3.2 g, 52%) as a white solid. 1H-NMR (CDCl3) δ 5.18 (s, 2H), 6.50 (dd, 1H), 6.76 (d, 1H), 6.80 (d, 1H), 7.22 (m, 1H), 7.64 (d, 1H), 7.73 (td, 1H), 8.55 (m, 1H); LCMS RT=0.89 min; [M+H]+=235.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08207172B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-f54bd1f54c5b4a04b92ab6e997ebd176
출처 메모uspto-grants-2012_06