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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 350539생성일: 2026년 10월 24일

4-Hydroxy-3-nitrobenzoic acid → Benzoic acid, 4-hydroxy-3-nitro-, methyl ester

https://huagongshe.com/ko/reaction/350539

반응식

참여 물질

역할이름HCID투입량
반응물4-Hydroxy-3-nitrobenzoic acidHCID 12033—
반응물TrimethylsilyldiazomethaneHCID 167693—
용매Benzene methanolHCID 21927730—
생성물Benzoic acid, 4-hydroxy-3-nitro-, methyl esterHCID 6683575.2%

반응 단계

To a stirred solution of 4-hydroxy-3-nitrobenzoic acid (5.18 g, 28.29 mmol) in benzene-MeOH (4:1, v/v, 140 mL) was added TMSCHN2 (14.10 mL, 28.20 mmol, 2 M solution in hexane) at room temp, and the resulting mixture was stirred overnight. The mixture was evaporated and the residue was purified by column chromatography on silica-gel with CHCl3 as eluent to give 4.18 g (75%) methyl 3-nitro-4-hydroxybenzoate as a yellow crystalline solid. 1H-NMR (CDCl3) δ 3.95 (s, 3H), 7.22 (d, 1H, J=8.8 Hz), 8.24 (dd, 1 , J=2.0, 8.8 Hz), 8.83 (d, 1H, J=2.0 Hz), 10.89 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07179819B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-3903681cc0ab4a48ab882859b262e667
출처 메모uspto-grants-2007_02