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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 444066생성일: 2026년 10월 25일

Acrylonitrile → 1,3-Di(n-hexadecyloxy)-2-(2-cyanoethylamino)propane

https://huagongshe.com/reaction/444066

반응식

참여 물질

역할이름HCID투입량
반응물AcrylonitrileHCID 7855—
반응물Sodium HydroxideHCID 14798—
반응물Tetrabutylammonium HydroxideHCID 2723671—
반응물1,3-Dihexadecyloxy-2-aminopropaneHCID 18427232—
생성물1,3-Di(n-hexadecyloxy)-2-(2-cyanoethylamino)propaneHCID 2346611936%

반응 조건

온도60 °C

반응 단계

A mixture of 1,3-di(n-hexadecyloxy)-2-aminopropane (500 mg., 0.93 mmoles), acrylonitrile (75 ml.) and 2 wt. % aqueous sodium hydroxide solution (75 ml.) was heated to 60° C. Tetrabutyl ammonium hydroxide (1 ml. of 40 wt. % aqueous solution) was then added and the resulting mixture stirred for 15 minutes at 90° C. The reaction mixture was then cooled, causing precipitation of solids, which were isolated by filtration and found (TLC) to contain a large quantity of unreacted starting material. Using fresh acrylonitrile and aqueous sodium hydroxide solution in each cycle, the solids were treated two more times by the above procedure. The third cycle solid product was purified by silica gel chromatography (elution with toluene:ethyl acetate) [200 mg., 36% yield, m.p. 45°-46° C., ir (CHCl3) 2250 cm-1, n.m.r. (CDCl3) δ 3.07 (t, 2, --NHCH2CH2CN) and 2.53 (t, 2, --NHCH2CH2CN)].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04262021
출처 데이터셋uspto-grants-1981_04
ORD IDord-9f7ada9aed584795bb0d96388af23805
출처 메모uspto-grants-1981_04