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Triethylamine → N-(3,7,11,15-Tetramethyl-2,6,10,14-hexadecatetraenoyl)-glycine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 反応物 | 3,7,11,15-Tetramethyl-2,6,10,14-hexadecatetraenic acid | HCID 128570 | — |
| 反応物 | Glycine ethyl ester, hydrochloride | HCID 2723640 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | N-(3,7,11,15-Tetramethyl-2,6,10,14-hexadecatetraenoyl)-glycine | HCID 54055783 | 85% |
反応手順
The reaction of 6.1 g of 3,7,11,15-tetramethyl-2,6,10,14-hexadecatetraenoic acid with glycine ethyl ester hydrochloride was conducted in the same manner as described in Example 1 except that 6.5 ml of triethylamine was used. Then, a solution of 2.7 g of potassium hydroxide in ethanol was added. The mixture was heated under reflux for 30 minutes. After the completion of the reaction, water was added and the obtained aqueous solution was extracted with ethyl acetate. The ethyl acetate layer was washed with water and dried over magnesium sulfate. The solvent was distilled off to afford 6.1 g (yield 85%) of the title compound as a pale brown oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04762829 |
| 出典データセット | uspto-grants-1988_08 |
| ORD ID | ord-1d5e702110244a0e832fd0d8c9e22490 |
| 出典メモ | uspto-grants-1988_08 |