Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Acetic Anhydride → trans-Racemic-2-phenylcyclohexyl acetate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Acetic Anhydride | HCID 7918 | — |
| 반응물 | rel-(1R,2S)-2-Phenylcyclohexanol | HCID 102793 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | Tin(II) trifluoromethanesulfonate | HCID 2776843 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | trans-Racemic-2-phenylcyclohexyl acetate | HCID 11009435 | — |
반응 단계
To a stirred solution of trans-racemic-2-phenylcyclohexanol (4.63 g, 26.3 mmol) and tin(II)trifluoromethanesulfonate (219 mg, 0.525 mmol) under nitrogen in anhydrous DCM (100 ml) at room temperature was added acetic anhydride (3.72 ml, 4.02 g, 39.4 mmol) in one portion. The mixture was stirred for 18 hours at room temperature. The mixture was poured into saturated aqueous sodium bicarbonate (200 ml). The mixture was extracted with DCM (2×200 ml). The combined organic layers were washed with brine (70 ml), dried over sodium sulfate, and concentrated under reduced pressure to provide the desired product as a light yellow oil. LC-MS: calculated for C14H18O2 218.29 observed m/e: 219.33 (M+H)+ (Rt 0.93/2 min)
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09290517B2 |
| 출처 데이터셋 | uspto-grants-2016_03 |
| ORD ID | ord-61acf6a0ada5406db8c9393079df05f7 |
| 출처 메모 | uspto-grants-2016_03 |