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HRID 1106作成日:2026年10月23日

Ethanolamine → Monosodium 2-(2-hydroxy-3-tetradecyloxypropylamino)ethyl phosphate

https://huagongshe.com/ja/reaction/1106

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolamineHCID 700—
反応物Phosphoric AcidHCID 1004—
反応物TetrahydrofuranHCID 8028—
反応物Sodium HydroxideHCID 14798—
反応物Phosphorus oxide (P4O10)HCID 14812—
反応物Oxirane, 2-((tetradecyloxy)methyl)-HCID 38190—
反応物SodiumHCID 5360545—
反応物3-(2-Hydroxyethylamino)-1-tetradecyloxy-2-propanolHCID 12458863—
溶媒WaterHCID 962—
生成物Monosodium 2-(2-hydroxy-3-tetradecyloxypropylamino)ethyl phosphateHCID 8830241536.2%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US05723497
出典データセットuspto-grants-1998_03
ORD IDord-1c432984f9d54ac78349420a214a1024
出典メモuspto-grants-1998_03