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HRID 10176作成日:2026年10月24日

Water → acetophenone O-[2-((morpholin-4-yl))ethyl]oxime

https://huagongshe.com/ja/reaction/10176

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium HydroxideHCID 14798—
反応物AcetophenonoximeHCID 69185—
反応物Morpholine, 4-(2-chloroethyl)-, hydrochloride (1:1)HCID 77210—
触媒Tetrabutylammonium BromideHCID 74236—
溶媒TolueneHCID 1140—
生成物acetophenone O-[2-((morpholin-4-yl))ethyl]oximeHCID 86594237—

反応条件

温度75 °C

反応手順

To a solution of acetophenone oxime (20 g) in toluene (700 mL) was added subsequently tetrabutylammonium bromide (4.77 g), water (8 mL), 4-(2-chloroethyl)morpholine hydrochloride (30.31 g) and finally 50% sodium hydroxide (aq, 52 mL). The resulting mixture was heated at 75° C. overnight. After cooling to room temperature water was added, to dissolve all the salts, the layers were separated, and the aqueous layer was extracted with toluene. The organic layers were dried (MgSO4), and concentrated in vacuo. The residue was purified by flash chromatography (SiO2, CH2Cl2/MeOH 95/5) to afford acetophenone O-[2-((morpholin-4-yl))ethyl]oxime as an oil. The obtained oil was dissolved in 6M HCl (aq, 500 mL) and heated under reflux for 5 hours and subsequently stirred overnight at room temperature. The mixture was extracted with ether and concentrated in vacuo. The residue was crystallized from ethanol, to afford O-[2-((morpholin-4-yl))ethyl]hydroxylamine dihydrochloride. 24.8 g (77%)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07094779B2
出典データセットuspto-grants-2006_08
ORD IDord-7cdc52eb0f104415883f65036a3b8c9b
出典メモuspto-grants-2006_08