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HRID 221518생성일: 2026년 10월 26일

2,3-Dinitrophenol → 1-Methoxy-2,3-dinitrobenzene

https://huagongshe.com/reaction/221518

반응식

참여 물질

역할이름HCID투입량
반응물2,3-DinitrophenolHCID 6191—
반응물Methyl iodideHCID 6328—
반응물Potassium CarbonateHCID 11430—
생성물1-Methoxy-2,3-dinitrobenzeneHCID 242825100%

반응 단계

A mixture of 2,3-dinitrophenol (5.43 mmol, 1 g), iodomethane (21.7 mmol, 1.35 mL) and K2CO3 (21.7 mmol, 2.99 g) was stirred at room temperature for 14 h. The reaction was then filtered through celite and the filter bed was washed with additional acetone. The filtrate was concentrated to provide 2,3-dinitroanisole (100%), which was dissolved in a mixture of EtOH/H2O (1:1, 20 mL) and Fe (19.4 mmol, 1.06 g) and concentrated HCl (8 drops) was added. The mixture was refluxed for 90 min., after which it was filtered through celite and the filter bed was washed with additional EtOH. The filtrate was concentrated and basified (pH>12) with 4 M NaOH and the aqueous layer was extracted with CH2Cl2. The organic phase was then separated and washed with brine, dried MgSO4 and concentrated to provide 2,3-diaminoanisole 36b (0.65 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08207173B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-c09bce2eeafa489c83187f3b7a592430
출처 메모uspto-grants-2012_06