戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 73648作成日:2026年10月24日

N,N,N',N'-Tetramethylazodicarboxamide → O-(Diphenylphosphinyl)hydroxylamine

https://huagongshe.com/ja/reaction/73648

反応式

関与物質

役割名称HCID仕込み量
反応物N,N,N',N'-TetramethylazodicarboxamideHCID 4278—
反応物Sodium HydroxideHCID 14798—
反応物Diphenylphosphinic chlorideHCID 73910—
反応物Hydroxyamine hydrochlorideHCID 443297—
溶媒WaterHCID 962—
溶媒1,4-DioxaneHCID 31275—
生成物O-(Diphenylphosphinyl)hydroxylamineHCID 1095545382.5%

反応条件

温度0 °C

反応手順

A 5 L 4-neck round bottom flask (rbf) fitted with an overhead stirrer & a thermocouple was charged with; (1) a solution of NaOH (60.85 g, 1.52 mol, 2.4 eq) in 180 mL water, (2) a solution of hydroxylamine-HCl (110.12 g, 1.58 mol, 2.5 eq) in 180 mL water and (3) 180 mL dioxane. The mixture was cooled in an ice/acetone bath to 0° C. 150 g of ice was added, followed by a precooled (to about 10° C.) solution of diphenylphosphinic chloride (150.0 g, 0.634 mol, 1 eq) in 180 mL dioxane (added all at once). The reaction became very thick with a white precipitate, requiring vigorous stirring. The internal temperature rose to 22° C. After 5 additional minutes stirring (10 minutes maximum), the reaction mixture was diluted with 2.5 L of ice cold water and filtered thru a large fritted funnel (15 cm diameter). The crude material was left on the frit to drain for one hour, then transferred back into the 5 L rbf. The solid was suspended in 500 mL ice cold 0.25N NaOH solution and vigorously stirred for five minutes (no more than 10 min), then filtered again, washing 2× with ice cold water and left to dry overnight on the fritted filter. The partially dried material was dried for 12 h in a vacuum oven (50° C., 0.1 torr) and then well crushed with a mortar & pestal. An additional 16 h of drying in the vacuum oven afforded 122 g (82%) the above compound as a white powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08829185B2
出典データセットuspto-grants-2014_09
ORD IDord-b2e4355bacd546f2952490ef96acf714
出典メモuspto-grants-2014_09