戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 23813作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Hydroxyamine hydrochlorideHCID 443297—
反応物Sodium AcetateHCID 517045—
反応物2,3-dichloro-N-(2-oxo-ethyl)-benzamideHCID 12133904—
溶媒MethanolHCID 887—
生成物2,3-Dichloro-N-{2-[formyl(Hydroxy)amino]ethyl}benzamideHCID 983848896%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06852882B2
出典データセットuspto-grants-2005_02
ORD IDord-7dd96b6db9174f8eb3739fca06e77bee
出典メモuspto-grants-2005_02