돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2395526생성일: 2026년 10월 25일

Ethylene Oxide → Emulphor

https://huagongshe.com/reaction/2395526

반응식

참여 물질

역할이름HCID투입량
반응물Ethylene OxideHCID 6354—
반응물TriethylamineHCID 8471—
반응물Oleyl AlcoholHCID 5284499—
용매1,4-DioxaneHCID 31275—
생성물EmulphorHCID 5364713—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05489303
출처 데이터셋uspto-grants-1996_02
ORD IDord-233b1cd5d651433e9f51fda2ef6d0953
출처 메모uspto-grants-1996_02