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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1041812생성일: 2026년 10월 27일

Formaldehyde → 4-(2-Hydroxy-ethyl)-3-nitro-benzoic acid tert-butyl ester

https://huagongshe.com/reaction/1041812

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물Tert-butyl 4-methyl-3-nitrobenzoateHCID 22451886—
반응물Potassium tert-butoxideHCID 23665647—
용매Dimethyl SulfoxideHCID 679—
생성물4-(2-Hydroxy-ethyl)-3-nitro-benzoic acid tert-butyl esterHCID 57853794665.1%

반응 단계

A solution of 4-methyl-3-nitro-benzoic acid tert-butyl ester (8.66 g, 36.5 mmol) in anhydrous DMSO (135 mL) was treated with paraformaldehyde (1.32 g, 44.0 mmol, 1.2 eq.) followed by t-BuOK (0.32 g, 2.7 mmol, 0.074 eq.). The mixture was stirred at room temperature for 2.5 h and quenched with aqueous NH4Cl (250 mL). The mixture was extracted with ethyl acetate (3×50 mL) and the combined organic layers were washed with brine and water, and then dried (Na2SO4) and concentrated. Silica gel chromatography using ethyl acetate (0→30%) in dichloromethane provided 4-(2-hydroxy-ethyl)-3-nitro-benzoic acid tert-butyl ester (4.8 g, white solid): 1H NMR (400 MHz, CDCl3) δ 8.47 (d, 1H), 8.13 (dd, 1H), 7.49 (d, 1H), 3.96 (q, 2H), 3.20 (t, 2H), 1.60 (s, 9H), and 4-(2-hydroxy-1-hydoxymethyl-ethyl)-3-nitro-benzoic acid tert-butyl ester (3.7 g, white solid): 1H NMR (400 MHz, CDCl3) δ 8.35 (d, 1H), 8.15 (dd, 1H), 7.65 (d, 1H), 4.05 (t, 4H), 3.61 (Q, 1H), 2.05 (t, 2H), 1.59 (s, 9H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08552186B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-170ce9f6c52a4a5fb91e55f7bbe18817
출처 메모uspto-grants-2013_10