戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1383750作成日:2026年10月27日

Potassium Iodide → Phosphoric Acid di-tert-butyl Ester 2,5-dioxo-4,4-diphenyl-imidazolidin-1-ylmethyl Ester

https://huagongshe.com/reaction/1383750

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物Potassium CarbonateHCID 11430—
反応物3-(Chloromethyl)-5,5-diphenylimidazolidine-2,4-dioneHCID 11098633—
反応物Potassium di-tert-butyl phosphateHCID 23674467—
溶媒AcetonitrileHCID 6342—
生成物Phosphoric Acid di-tert-butyl Ester 2,5-dioxo-4,4-diphenyl-imidazolidin-1-ylmethyl EsterHCID 1545954538.6%

反応条件

温度0 °C

反応手順

35.5 Grams of 3-(chloromethyl)-5,5-diphenyl-2,4-imidazolidinedione from Step (A), 30.7 g of potassium di(t-butyl) phosphate, 0.6 g of potassium carbonate, and 0.15 g of potassium iodide were slurried into 200 mL acetonitrile. The reaction mixture was heated at reflux for 2.5 hours. The solution was filtered to remove potassium chloride precipitate. The filtrate was cooled to 0° C. and filtered to give 22.3 g of the title compound (38.6% yield); mp 108.5° C. (d). 1H NMR (DMSO-d6): 1.3 ppm (s, 18H), 5.2 (d, 2H), 7.3-7.5 (m, 10H), 9.9 (s, 1H); doublet from long range phosphorus coupling.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06255492B1
出典データセットuspto-grants-2001_07
ORD IDord-92da913ed7284ceca65d24fa3ae26c6d
出典メモuspto-grants-2001_07