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HRID 483991作成日:2026年10月25日

Acetic Acid → 3-(p-Chlorobenzylamino)propyl(diethoxymethyl)phosphinic acid ethyl ester

https://huagongshe.com/reaction/483991

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物4-ChlorobenzaldehydeHCID 7726—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物Phosphinic acid, (3-aminopropyl)(diethoxymethyl)-, ethyl esterHCID 10422382—
溶媒MethanolHCID 887—
生成物3-(p-Chlorobenzylamino)propyl(diethoxymethyl)phosphinic acid ethyl esterHCID 54432946—

反応手順

1.41 g of p-chlorobenzaldehyde are added to a solution of 2.53 g of 3-aminopropyl(diethoxymethyl)phosphinic acid ethyl ester in 10 ml of anhydrous methanol, and the resulting clear solution is stirred at room temperature for 30 minutes. There are then added first 0.6 g of glacial acetic acid and then, dropwise, 0.21 g of sodium cyanoborohydride in solution in 5 ml of methanol. An exothermic reaction begins. The mixture is stirred at 20° for 3 hours and adjusted to pH 8, and the solvent is removed. The residue is dissolved in dichloromethane and washed with water. The organic phase is separated off, dried over sodium sulfate and concentrated to dryness by evaporation. The oil that remains is purified by chromatography on silica gel, yielding 3-(p-chlorobenzylamino)propyl(diethoxymethyl)phosphinic acid ethyl ester in the form of a yellowish oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05229379
出典データセットuspto-grants-1993_07
ORD IDord-0a7d03df098d4b8fbfac141aa4c9c907
出典メモuspto-grants-1993_07