化工社化工社 化学情報印刷レポート · 研究参考用
1,3-Propanediol → 1-(z,z,z,z,z,z-Docosa-4,7,10,13,16,19-hexaenoyloxy)-3-hydroxypropane
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1,3-Propanediol | HCID 10442 | — |
| 反応物 | Dicyclohexylcarbodiimide | HCID 10868 | — |
| 反応物 | Doconexent | HCID 445580 | — |
| 触媒 | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 1-(z,z,z,z,z,z-Docosa-4,7,10,13,16,19-hexaenoyloxy)-3-hydroxypropane | HCID 86758951 | — |
反応手順
A solution of z,z,z,z,z,z-docosa-4,7,10,13,16,19-hexaenoic acid (6.4 g, 19.5 mmol) in methylene chloride (225 ml) was added dropwise to a solution of 1,3-propane diol (7.5 g, 99 mmol), 1,3-dicyclohexylcarbodiimide (4.65 g, 20 mmol) and 4-(N,N-dimethylamino)pyridine (2.1 g, 17 mmol) in methylene chloride (225 ml) at −10° C. The reaction mixture was stirred overnight, warming up to room temperature. The reaction was filtered, concentrated and purified by flash chromatography (ethyl acetate/hexane) to yield 1-(z,z,z,z,z,z-docosa-4,7,10,13,16,19-hexaenoyloxy)-3-hydroxypropane as a pale yellow oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | USRE040480E1 |
| 出典データセット | uspto-grants-2008_09 |
| ORD ID | ord-ba77b7c555334b5fb024de271e85041c |
| 出典メモ | uspto-grants-2008_09 |