Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Diethyl Ether → Cyclohexanol, 1-ethynyl-, 1-acetate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Diethyl Ether | HCID 3283 | — |
| 반응물 | 1-Ethynylcyclohexanol | HCID 6525 | — |
| 반응물 | Acetic Anhydride | HCID 7918 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 촉매 | Scandium(III) triflate | HCID 2734571 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | Cyclohexanol, 1-ethynyl-, 1-acetate | HCID 78903 | 110.7% |
반응 단계
To 3.1 g (25 mmol) 1-ethynyl-1-cyclohexanol in 25 ml acetonitrile were added 7.1 ml (75 mmol, 3 eq) acetic anhydride at −20° C. 12.3 mg (0.03 mmol) scandiumtriflate in 300 μl THF were added and the solution was stirred for 2 h. Additional 12.3 mg (0.03 mmol) scandiumtriflate in 300 μl THF were added and stirring was continued for 30 min. A saturated aqueous solution of NaHCO3 and ether were added. The layers were separated and the inorganic one was extracted with ether. The combined organic phases were washed with brine and dried over Na2SO4. Evaporation yielded 4.6 g crude 1-ethynylcyclohexyl acetate as colorless oil, MS: 166 (M).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07449483B2 |
| 출처 데이터셋 | uspto-grants-2008_11 |
| ORD ID | ord-a67f1e0cc08c4f6a98f30aa3663cf99f |
| 출처 메모 | uspto-grants-2008_11 |