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HRID 1166582作成日:2026年10月26日

Hydroxyamine hydrochloride → 1-[5-Hydroxy-3-(Hydroxymethyl)-2,3-Dihydro-1,4-Benzodioxin-6-yl]-1-Ethanone Oxime

https://huagongshe.com/reaction/1166582

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Pyridine ethanolHCID 21975839—
反応物1-[(3S)-5-hydroxy-3-(hydroxymethyl)-2,3-dihydro-1,4-benzodioxin-6-yl]-1-EthanoneHCID 69017006—
溶媒EthanolHCID 702—
生成物1-[5-Hydroxy-3-(Hydroxymethyl)-2,3-Dihydro-1,4-Benzodioxin-6-yl]-1-Ethanone OximeHCID 136343266—

反応手順

A solution of hydroxylamine hydrochloride (2,38 g, 34.2 mmole) in 1:1 ethanol/pyridine (100 mL) was added to a solution of 1-[(3S)-5-hydroxy-3-(hydroxymethyl)-2,3-dihydro-1,4-benzodioxin-6-yl]-1-ethanone (1.92 g, 8.57 mmole) in ethanol (200 mL). It was then heated to reflux under nitrogen for 5 hours. Upon cooling, the solvent was removed and replaced with ethyl acetate. The solution was then washed with water (200 mL) and with aqueous 2N HCl (100 mL), dried over magnesium sulfate, filtered and evaporated in vacuum to give 1.89 g (93%) of the (S)-enantiomer of the title compound as a gray solid, m.p. 162°C. MS (ESI) m/z 240 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06613913B2
出典データセットuspto-grants-2003_09
ORD IDord-1329ffc6bb7d45579e3a712a8a68c426
出典メモuspto-grants-2003_09