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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 275489생성일: 2026년 10월 25일

Oxamic Acid → N-[2-(3,4-Dimethoxyphenyl)ethyl]-N-hydroxyoxamide

https://huagongshe.com/reaction/275489

반응식

참여 물질

역할이름HCID투입량
반응물Oxamic AcidHCID 974—
반응물4-MethylmorpholineHCID 7972—
반응물Ethyl chloroformateHCID 10928—
반응물Ammonium ChlorideHCID 25517—
반응물N-[2-(3,4-dimethoxyphenyl)ethyl]-N-hydroxyamineHCID 20088217—
용매1,2-DimethoxyethaneHCID 8071—
생성물N-[2-(3,4-Dimethoxyphenyl)ethyl]-N-hydroxyoxamideHCID 1523286517.4%

반응 단계

N-[2-(3,4-Dimethoxyphenyl)ethyl]-N-hydroxamide. To a suspension of oxamic acid (195 mg, 2.21 mmol) in 1,2-dimethoxyethane (7 mL) under an argon atmosphere was added dropwise N-methylmorpholine (0.27 mL, 2.42 mmol), followed by ethyl chloroformate (0.23 mL, 2.42 mmol). After stirring for 1 h at room temperature, a solution of N-[2-(3,4-dimethoxyphenyl)ethyl]-N-hydroxyamine (417 mg, 2.10 mmol) in 1,2-dimethoxyethane (5 mL) was added, and the resulting mixture was stirred for 4 h. Saturated aqueous ammonium chloride was added, and the mixture was extracted with methylene chloride (2×). The combined organic extracts were washed successively with 10% hydrochloric acid and water and dried (potassium carbonate). The solvent was removed in vacuo and the residue was purified by flash chromatography, eluting with 5% methanol/methylene chloride, and recrystallized from methanol/methylene chloride to provide the oxamide (98 mg, 17%): m.p. 143°-144° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05393788
출처 데이터셋uspto-grants-1995_02
ORD IDord-f405f2584e0644dc9937b8412f330290
출처 메모uspto-grants-1995_02