Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Ammonium Chloride → (1R,4R)-4-phenylcyclopent-2-enol
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | 4-Cyclopentene-1,3-diol, 1-acetate, (1R,3S)-rel- | HCID 9855498 | — |
| 반응물 | HCID 178418546 | HCID 178418546 | — |
| 반응물 | HCID 178478979 | HCID 178478979 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (1R,4R)-4-phenylcyclopent-2-enol | HCID 13613834 | 84% |
반응 단계
A solution of (1R,4S)-4-acetoxy-2-cyclopenten-1-ol (491 mg, 3.45 mmol), THF (10 mL), and copper(I) cyanide (93 mg, 1.04 mmol) was cooled to <−20° C. and phenylmagnesium chloride (2.0 M in THF, 5.18 mL, 10.4 mmol) was added at the same temperature. After 10 minutes, TLC (50% EtOAc/hexanes) showed complete conversion. Saturated aqueous NH4Cl (50 mL) was added, extracted with EtOAc (3×50 mL), and dried (Na2SO4) the combined organic layers. Concentrated and purified the residue by flash column chromatography (10-50% EtOAc/hexanes, gradient elution), to provide the title compound (463 mg, 2.89 mmol, 84%). MS (DCI) m/z 143 (M−OH)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08802711B2 |
| 출처 데이터셋 | uspto-grants-2014_08 |
| ORD ID | ord-5fcbdfb42e2d4cc385125cd8f721f81d |
| 출처 메모 | uspto-grants-2014_08 |