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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 354337생성일: 2026년 10월 25일

Benzyl 2-nitrophenyl ether → 2-Benzyloxyaniline

https://huagongshe.com/reaction/354337

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl 2-nitrophenyl etherHCID 736266—
반응물Sodium borohydrideHCID 4311764—
촉매Nickel DichlorideHCID 24385—
용매MethanolHCID 887—
생성물2-BenzyloxyanilineHCID 240548100%

반응 단계

To a stirred solution of 2-benzyloxynitrobenzene (9.92 g, 43.3 mmol) and NiCl2 (20.3 g, 157 mmol) in MeOH (350 mL) was added portionwise NaBH4 (8.09 g, 214 mmol) at 0° C. After disappearing of the starting material (monitored by TLC), the mixture was evaporated off. The black precipitate was dissolved in 1N HCl, then acidic solution was alkalified by the addition of 1N NaOH and extracted with EtOAc. The extracts were washed brine, dried over Na2SO4, and concentrated to dryness. Chromatography of the residue with CHCl3 as eluent gave 2-benzyloxy aniline (8.60 g, 100%) as a reddish oil. 1H-NMR (CDCl3) δ3.71 (broad s, 2H), 5.06 (s, 2H), 6.68-6.86 (m, 4H), 7.32-7.44 (m, 5H); FAB-MS m/z 200 (M++1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06756378B2
출처 데이터셋uspto-grants-2004_06
ORD IDord-50a53959db354bfd9338cafbe55baa10
출처 메모uspto-grants-2004_06