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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 350400생성일: 2026년 10월 26일

2-Nitrophenol → Benzyl 2-nitrophenyl ether

https://huagongshe.com/reaction/350400

반응식

참여 물질

역할이름HCID투입량
반응물2-NitrophenolHCID 6947—
반응물Benzyl BromideHCID 7498—
반응물Potassium CarbonateHCID 11430—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물Benzyl 2-nitrophenyl etherHCID 73626689.1%

반응 단계

To a stirred solution of 2-nitrophenol (10.0 g, 72.0 mmol) and K2CO3 (9.96 g, 72.0 mmol) in DMF (150 mL) was added dropwise benzyl bromide (9.40 mL, 79.2 mmol) at 0° C. After being stirred at room temperature for 3 hr, the reaction mixture was diluted with water, which was extracted with Et2O. The extracts were washed with brine, dried over Na2SO4, and concentrated to dryness. Chromatography of the residue with hexane-EtOAc (2:1, v/v) as eluent gave 2-benzyloxy nitrobenzene (14.7 g, 89%) as a yellow oil. 1H-NMR (CDCl3) δ 5.24 (s, 2H), 7.04 (t, J=7.8 Hz, 1H), 7.12 (d, J=7.8 Hz, 1H), 7.31–7.50 (m, 5H), 7.51 (d, J=1.5 Hz, 1H), 7.86 (dd, J=7.8, 1.5 Hz, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07179819B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-d5f3d3fbc1a94eb296a614a0e529ce09
출처 메모uspto-grants-2007_02