Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Methyl iodide → 2,2-Dimethylcyclohexan-1-one
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Methyl iodide | HCID 6328 | — |
| 반응물 | Triethylborane | HCID 7357 | — |
| 반응물 | 2-Methylcyclohexanone | HCID 11419 | — |
| 반응물 | Potassium hydride | HCID 82127 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2,2-Dimethylcyclohexan-1-one | HCID 136929 | — |
반응 단계
A suspension of potassium hydride (5.5 mmol) and 2-methylcyclohexanone (5 mmol) in dry tetrahydrofuran (10 ml) is stirred for 30 mins at room temperature. Triethylborane (6.25 mmol) is slowly added dropwise and the mixture is stirred for 16 hours at room temperature. After addition of methyl iodide stirring is continued for another 8 hours, the reaction is then quenched with saturated aqueous ammonium chloride solution and twice extracted with diethyl ether. The combined organic phases are dried over sodium sulphate and concentrated to dryness in a vacuum and produce the title compound, which can be reacted without [without] purification (JACS 1985, 107, 19, 5391-5396).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07727979B2 |
| 출처 데이터셋 | uspto-grants-2010_06 |
| ORD ID | ord-86101b2e7f9945179d50d853ef03d403 |
| 출처 메모 | uspto-grants-2010_06 |