Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Bromoacetonitrile → 7-Cyano-5-oxoheptanoic acid
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Bromoacetonitrile | HCID 11534 | — |
| 반응물 | 4-Acetylbutyric acid | HCID 18407 | — |
| 반응물 | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 7-Cyano-5-oxoheptanoic acid | HCID 14986712 | — |
반응 단계
To a solution of potassium hexamethyldisilazide (66 ml, 60 mmol) in dry tetrahydrofuran (140 ml) at -70° is added slowly 5-oxohexanoic acid (36 ml, 30 mmol). The resulting yellow suspension is stirred at -70° for 1 h and bromoacetonitrile (2.2 ml, 32 mmol) is added slowly. The reaction mixture is stirred at -70° for 1 h and then at room temperature for 0.5 h. The reaction is quenched by addition of 1N aqueous hydrochloric acid (100 ml). The aqueous layer is extracted twice with ether. Combined organic layer is dried, filtered and evaporated to obtain a dark oil which is purified by silica gel chromatography using 9:1 ether/hexane with 1% acetic acid as eluent to give 7-cyano-5-oxoheptanoic acid as an oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05153214 |
| 출처 데이터셋 | uspto-grants-1992_10 |
| ORD ID | ord-8b89643d0bdd44568e4cd81cca446028 |
| 출처 메모 | uspto-grants-1992_10 |