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Hydroxyamine hydrochloride → 1-[5-Hydroxy-3-(Hydroxymethyl)-2,3-Dihydro-1,4-Benzodioxin-6-yl]-1-Ethanone Oxime
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydroxyamine hydrochloride | HCID 443297 | — |
| 反応物 | Pyridine ethanol | HCID 21975839 | — |
| 反応物 | 1-[(3S)-5-hydroxy-3-(hydroxymethyl)-2,3-dihydro-1,4-benzodioxin-6-yl]-1-Ethanone | HCID 69017006 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 1-[5-Hydroxy-3-(Hydroxymethyl)-2,3-Dihydro-1,4-Benzodioxin-6-yl]-1-Ethanone Oxime | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07419986B2 |
| 出典データセット | uspto-grants-2008_09 |
| ORD ID | ord-a66de3d2330c46b1bac32853f6bae08a |
| 出典メモ | uspto-grants-2008_09 |