関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Isopropanol | HCID 3776 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | 1-Dodecyl glycidyl ether | HCID 17163 | — |
| 反応物 | L-Lysine monohydrochloride | HCID 69568 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | Nepsilon-(2-hydroxy-3-dodecyloxy)propyl-L-lysine hydrochloride | HCID 21309924 | 23.7% |
反応手順
L-lysine hydrochloride (18.3 g, 0.1 mols) and 2.0 g (0.2 mols) of sodium hydroxide were dissolved in 100 ml of water in a three-necked round flask, and 100 ml of i-propanol were added thereto. Then, 24.2 g (0.1 mols) of dodecylglycidyl ether were added dropwise thereto over a period of 30 minutes while being heat-refluxed and stirred. Further, the mixture was stirred under reflux for 3 hours. It was identified through TLC and gas chromatography that dodecylglycidyl ether disappeared. Thereafter, the resulting mixture was neutralized with 10.1 g (0.1 mols) of 36% hydrochloric acid. The reaction solution was concentrated under reduced pressure, and the residue was purified through silica-gel column chromatography (Kieselgel 60, eluent=mixture of chloroform, methanol and acetic acid at a ratio of 3:1:0.5) to give 10.1 g of Nε-(2-hydroxy-3-dodecyloxy)propyl-L-lysine hydrochloride (yield 23.7%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05919748 |
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| 出典データセット | uspto-grants-1999_07 |
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| ORD ID | ord-6dd2fa8946a6404589d27cb3909516c7 |
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| 出典メモ | uspto-grants-1999_07 |
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