関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Acetic Acid | HCID 176 | — |
| 反応物 | 4-Chlorobenzaldehyde | HCID 7726 | — |
| 反応物 | Sodium cyanoborohydride | HCID 5003444 | — |
| 反応物 | Phosphinic acid, (3-aminopropyl)(diethoxymethyl)-, ethyl ester | HCID 10422382 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 3-(p-Chlorobenzylamino)propyl(diethoxymethyl)phosphinic acid ethyl ester | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05229379 |
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| 出典データセット | uspto-grants-1993_07 |
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| ORD ID | ord-0a7d03df098d4b8fbfac141aa4c9c907 |
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| 出典メモ | uspto-grants-1993_07 |
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