참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acrylonitrile | HCID 7855 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Tetrabutylammonium Hydroxide | HCID 2723671 | — |
| 반응물 | 1,3-Dihexadecyloxy-2-aminopropane | HCID 18427232 | — |
| 생성물 | 1,3-Di(n-hexadecyloxy)-2-(2-cyanoethylamino)propane | HCID 23466119 | 36% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04262021 |
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| 출처 데이터셋 | uspto-grants-1981_04 |
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| ORD ID | ord-9f7ada9aed584795bb0d96388af23805 |
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| 출처 메모 | uspto-grants-1981_04 |
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