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HRID 973629作成日:2026年10月25日

N-(2,3-Epoxypropyl)phthalimide → 3-Aminopropyl(2-hydroxy-3-phthalimido-propyl)phosphinic acid

https://huagongshe.com/reaction/973629

反応式

関与物質

役割名称HCID仕込み量
反応物N-(2,3-Epoxypropyl)phthalimideHCID 21601—
反応物3-Amino-propanephosphonousHCID 9989268—
触媒zinc(II)iodideHCID 9883512—
溶媒Hydrochloric AcidHCID 313—
溶媒HexamethyldisilazaneHCID 13838—
生成物3-Aminopropyl(2-hydroxy-3-phthalimido-propyl)phosphinic acidHCID 9901853—

反応手順

A suspension of 2.46 g of 3-aminopropylphosphonous acid in 20 ml of hexamethyldisilazane is heated to reflux under an inert atmosphere for 24 hours after which a clear solution results. The excess hexamethyldisilazane is removed by distillation at atmospheric pressure under a slight positive pressure of inert gas to afford a colourless oil. The oil is cooled to circa 66° and treated with 0.64 g of anhydrous zinc iodide and 4.62 g of N-(2,3-epoxypropyl)phthalimide. An exothermic reaction occurs. The reaction mixture is refluxed for 6 hours after which time thin layer chromatography indicates the reaction to be complete. The reaction mixture is filtered and the filtrate evaporated to dryness in vacuo at 40°. The residue is dissolved in water and stirred at room temperature for 1 hour and the water removed in vacuo to give an oily solid. This is dissolved in 25 ml of 2.0M aqueous hydrochloric acid and washed with dichloromethane and ether. Removal of the water at 40° in vacuo affords a brown solid which is purified by ion-exchange chromatography on DOWEX® 50 W×8 (14-40 mesh) to give 3-aminopropyl(2-hydroxy-3-phthalimido-propyl)phosphinic acid, m.p. 268°-71°, as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05064819
出典データセットuspto-grants-1991_11
ORD IDord-91cc953306554c4786a4dcfdd7874f61
出典メモuspto-grants-1991_11