Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Acetonitrile → Methyl (RS)-4-cyano-2-phenylbutanoate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Acetonitrile | HCID 6342 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | Methyl atropate | HCID 193334 | — |
| 반응물 | Lithium diisopropylamide | HCID 2724682 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Cyclohexane | HCID 8078 | — |
| 생성물 | Methyl (RS)-4-cyano-2-phenylbutanoate | HCID 53645094 | 75% |
반응 단계
Lithium diisopropylamide (3.67 ml of a 1.5 molar solution in cyclohexane) was added to acetonitrile (0.26 ml) in tetrahydrofuran (10 ml) at -78° C. After 1 hour, methyl 2-phenyl-acrylate (see Preparation 22) (0.81 g) in tetrahydrofurn (10 ml) was added and the mixture was stirred for 1 hour, allowed to warm to room temperature then treated with saturated ammonium chloride solution. The resulting mixture was partitioned between ethyl acetate and water, the organic phase dried over magnesium sulphate and evaporated to give a residue which was partitioned between ether and 10% aqueous sodium carbonate. The organic layer was dried over magnesium sulphate and evaporated to leave the title compound (0.5 g, 75%) as an oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05292749 |
| 출처 데이터셋 | uspto-grants-1994_03 |
| ORD ID | ord-80af75f55504407f8422051aeb00f6fc |
| 출처 메모 | uspto-grants-1994_03 |