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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 23813생성일: 2026년 10월 24일

Hydroxyamine hydrochloride → 2,3-Dichloro-N-{2-[formyl(Hydroxy)amino]ethyl}benzamide

https://huagongshe.com/ko/reaction/23813

반응식

참여 물질

역할이름HCID투입량
반응물Hydroxyamine hydrochlorideHCID 443297—
반응물Sodium AcetateHCID 517045—
반응물2,3-dichloro-N-(2-oxo-ethyl)-benzamideHCID 12133904—
용매MethanolHCID 887—
생성물2,3-Dichloro-N-{2-[formyl(Hydroxy)amino]ethyl}benzamideHCID 983848896%

반응 단계

To a solution of 2,3-dichloro-N-(2-oxo-ethyl)-benzamide (33 g, 0.14 mol) in MeOH (500 mL) was added hydroxylamine hydrochloride (20 g, 0.28 mol) and sodium acetate (23.6 g, 0.28 mol). The mixture was stirred 1.5 h and the MeOH was removed in vacuo. The residue was partioned between saturated NaHCO3 (200 mL) and dichloromethane/MeOH (9:1; 100 mL). The aqueous layer was extracted (4×100 mL) with dichloromethane/MeOH (9:1). The combined organic extracts were washed with brine (50 mL), were dried (Na2SO4) and were concentrated to provide the title compound (34.3 g, 96%) as a 1:1 mixture of cis and trans isomers as a clear, pale brown oil. 1H NMR (400 MHz, CD3OD): δ 7.66 (m, 1H); 7.45 (m, 3H); 6.78 (t, j=4.1 Hz, 0.5H); 4.30 (d, j=4.1 Hz, 1H); 4.12 (d, j=5.3 Hz, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06852882B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-7dd96b6db9174f8eb3739fca06e77bee
출처 메모uspto-grants-2005_02