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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 222040생성일: 2026년 10월 25일

4-Benzyloxy-3-chloronitrobenzene → 4-Benzyloxy-3-chloroaniline

https://huagongshe.com/reaction/222040

반응식

참여 물질

역할이름HCID투입량
반응물4-Benzyloxy-3-chloronitrobenzeneHCID 308509—
촉매IronHCID 23925—
용매Acetic AcidHCID 176—
생성물4-Benzyloxy-3-chloroanilineHCID 126828588.1%

반응 단계

1-Benzyloxy-2-chloro-4-nitrobenzene (10.0 g, 37.9 mmol) and iron powder (10.6 g, 189.6 mmol) were mixed in 250 mL acetic acid and were stirred at rt overnight. The reaction mixture was filtered through a pad of Celite®, and washed with EtOAc. The filtrate was concentrated in vacuo and neutralized with saturated Na2CO3 solution. The contents were extracted with EtOAc (6×300 mL). The combined organic layers were washed with brine, dried over MgSO4, filtered, and concentrated in vacuo. The resulting crude material was triturated with Hex/EtOAc (2:1) to furnish 4-Benzyloxy-3-chloro-phenylamine (7.8 g, 88%) as a white solid. 1H-NMR (DMSO-d6) δ 7.43-7.30 (m, 5H), 6.90 (d, 1H), 6.63 (d, 1H), 6.46 (dd, 1H), 4.99 (s, 2H), 4.92 (s, 2H); LCMS RT=2.09 min; [M+H]+=234.5.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08207172B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-2c92ca0611c24f42908c1d68d0a42869
출처 메모uspto-grants-2012_06