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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 43594생성일: 2026년 10월 23일

3-Methoxy-4-nitrobenzoic acid → N-(3-Methoxy-4-nitrobenzoyl)serine methyl ester

https://huagongshe.com/ko/reaction/43594

반응식

참여 물질

역할이름HCID투입량
반응물3-Methoxy-4-nitrobenzoic acidHCID 78764—
반응물DiisopropylethylamineHCID 81531—
반응물L-Serine, methyl ester, hydrochloride (1:1)HCID 2723730—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
생성물N-(3-Methoxy-4-nitrobenzoyl)serine methyl esterHCID 6754893969%

반응 단계

Dichloromethane (80 mL) was added to serine methyl ester hydrochloride (2.64 g, 17 mmol), 3-methoxy-4-nitrobenzoic acid (3 g, 15.2 mmol), WSC hydrochloride (3.83 g, 20 mmol), DMAP (0.18 g, 1.5 mmol) and N,N-diisopropylethylamine (2.58 g, 20 mmol), and the mixture was stirred at room temperature for one day. The reaction solution was washed with water and brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (elution solvent: ethyl acetate/hexane=1/2, 1/1, 2/1, 1/0) to obtain 3.11 g of the title compound as a colorless solid (69%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536197B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-44b331cbf319449888b2dd62743014fb
출처 메모uspto-grants-2013_09