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HRID 2395526作成日:2026年10月26日

Ethylene Oxide → Emulphor

https://huagongshe.com/reaction/2395526

反応式

関与物質

役割名称HCID仕込み量
反応物Ethylene OxideHCID 6354—
反応物TriethylamineHCID 8471—
反応物Oleyl AlcoholHCID 5284499—
溶媒1,4-DioxaneHCID 31275—
生成物EmulphorHCID 5364713—

反応手順

In 50 ml of dioxane, 20.00 g of polyethylene glycol monooleyl ether (average molecular weight 4,268) obtained by addition of ethylene oxide to an oleyl alcohol in the presence of an alkali catalyst and 1.90 g of triethyl amine were dissolved. The resultant solution and a solution of 1.85 g of p-toluenesulfonyl chloride in 10 ml of dioxane slowly added dropwise thereto were left reacting at 60° C. for two hours. The reaction product was refined by being dissolved with 200 ml of acetone added thereto, then cooled to 0° C., and left standing to allow sedimentation of the product aimed at. Then, a solution of 6.50 g of the product mentioned above in 30 ml of DMF and 0.55 g of potassium phthalimide added thereto were left reacting at 90° C. for two hours. The reaction product was refined by being dissolved with 60 ml of acetone added thereto, then cooled to 0° C., and left standing to allow sedimentation of the product aimed at. Subsequently, a solution of 6.00 g of the product mentioned above in 30 ml of ethanol and 1.00 g of hydrazinc hydrate added thereto were left reacting as refluxed for two hours. The reaction product was refined by being dissolved with 60 ml of acetone added thereto, then cooled to 0° C., and left standing to allow sedimentation of the product aimed at. Consequently, 5.20 g of an oleyl alcohol macromer possessed of amino groups at the terminals thereof was obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05489303
出典データセットuspto-grants-1996_02
ORD IDord-233b1cd5d651433e9f51fda2ef6d0953
出典メモuspto-grants-1996_02