Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Acrylonitrile → (2-Cyanoethyl)-alpha-naphthoxymalonic acid diethyl ester
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Acrylonitrile | HCID 7855 | — |
| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 반응물 | 4-Cyano-2(R,S)-alpha-naphthoxybutyric acid | HCID 23049648 | — |
| 반응물 | alpha-Naphthoxymalonic acid diethyl ester | HCID 54105534 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | (2-Cyanoethyl)-alpha-naphthoxymalonic acid diethyl ester | HCID 54279623 | — |
반응 단계
4-Cyano-2(R,S)-α-naphthoxybutyric acid: 0.11 ml of a 50% aqueous KOH solution is added at 0°, while stirring, to a mixture of 5.0 g of α-naphthoxymalonic acid diethyl ester and 1.09 ml of acrylonitrile. The reaction mixture is stirred for 5 days at room temperature and then dissolved in ethyl acetate. The ethyl acetate solution is washed with 2N sodium bicarbonate solution, 2N hydrochloric acid and brine, dried over sodium sulphate and concentrated by evaporation, leaving (2-cyanoethyl)-α-naphthoxymalonic acid diethyl ester.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04727060 |
| 출처 데이터셋 | uspto-grants-1988_02 |
| ORD ID | ord-0c2d879632c7416297f9a04382172ffc |
| 출처 메모 | uspto-grants-1988_02 |