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Nitrogen → 12-Hydroxy-N-{2-[(2-hydroxyethyl)amino]ethyl}octadecanamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Nitrogen | HCID 947 | — |
| 反応物 | Ethanol, 1-((2-aminoethyl)amino)- | HCID 174512 | — |
| 反応物 | 12-Hydroxystearic acid ethyl ester | HCID 3457651 | — |
| 反応物 | Sodium Methoxide | HCID 10942334 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 12-Hydroxy-N-{2-[(2-hydroxyethyl)amino]ethyl}octadecanamide | HCID 19694639 | 737.2% |
反応手順
A 30-ml two-necked flask equipped with a stirrer and dropping funnel was charged with 2.08 g (20 mmol) of aminoethylaminoethanol and 0.054 g (1 mmol) of sodium methoxide. While heating and stirring the contents at 80° C. in an N2 atmosphere, a solution of 3.29 g (10 mmol) of ethyl 12-hydroxystearate in 10 ml of THF was added dropwise over 2 hours. The resultant mixture was stirred further for 13 hours at 80° C. under reduced pressure. After completion of the reaction, the reaction mixture was poured into 500 ml of water, and precipitate formed was purified by flash column chromatography on silica gel, thereby obtaining 2.85 g (yield: 74%) of the title compound (IIf-1).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05723497 |
| 出典データセット | uspto-grants-1998_03 |
| ORD ID | ord-4e7d6fabfea64e0cb15c31ea61de1db0 |
| 出典メモ | uspto-grants-1998_03 |