関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethanolamine | HCID 700 | — |
| 反応物 | Phosphoric Acid | HCID 1004 | — |
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | Phosphorus oxide (P4O10) | HCID 14812 | — |
| 反応物 | Oxirane, 2-((tetradecyloxy)methyl)- | HCID 38190 | — |
| 反応物 | Sodium | HCID 5360545 | — |
| 反応物 | 3-(2-Hydroxyethylamino)-1-tetradecyloxy-2-propanol | HCID 12458863 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | Monosodium 2-(2-hydroxy-3-tetradecyloxypropylamino)ethyl phosphate | HCID 88302415 | 36.2% |
反応手順
A 300-ml flask equipped with a stirrer was charged with 5.13 g (14.8 mmol) of 3-(2-hydroxyethylamino)-1-tetradecyloxy-2-propanol prepared from tetradecyl glycidyl ether and ethanolamine in the same manner as in Preparation Example 14, and 70 mol of tetrahydrofuran, 1.95 g (16.9 mmol) of 85% phosphoric acid and 3.54 g (30.7 mmol) of P2O5 were added thereto. The resultant mixture was stirred at 65° C. for 10 hours. After cooling the mixture to room temperature, 0.56 g of water was added to the mixture, stirring was conducted for 30 minutes, 5.0 g of 48% aqueous NaOH were added further. After concentrating the resultant reaction mixture under reduced pressure, the resultant residue was subjected to extraction with ethanol by means of a Soxhlet's extractor. The resultant extract was concentrated under reduced pressure, and the residue was purified by column chromatography on silica gel, thereby obtaining 2.32 g (yield: 34.9%) of the title compound monosodium (IIa-14).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05723497 |
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| 出典データセット | uspto-grants-1998_03 |
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| ORD ID | ord-1c432984f9d54ac78349420a214a1024 |
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| 出典メモ | uspto-grants-1998_03 |
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