Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Triphenylphosphine → (3-(4-((1,3-Dioxolan-2-yl)methyl)benzyloxy)phenyl)-(phenyl)methanone
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Triphenylphosphine | HCID 11776 | — |
| 반응물 | 3-Hydroxybenzophenone | HCID 83050 | — |
| 반응물 | (4-((1,3-Dioxolan-2-yl)methyl)phenyl)methanol | HCID 86676898 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | (3-(4-((1,3-Dioxolan-2-yl)methyl)benzyloxy)phenyl)-(phenyl)methanone | HCID 71113108 | 117.8% |
반응 단계
To a cooled (0° C.) solution of (4-((1,3-dioxolan-2-yl)methyl)phenyl)methanol (0.45 g, 2.317 mmol), 3-hydroxybenzophenone (0.551 g, 2.78 mmol) and triphenylphosphine (0.729 g, 2.78 mmol) in anhydrous THF, di-iso-propylazodicarboxylate (1.027 mL, 2.78 mmol) was added dropwise. The reaction mixture was allowed to warm to RT and stirred at this temperature for 16 hours. The reaction mixture was diluted with ethyl acetate and washed with 10% aqueous potassium carbonate, brine and dried (magnesium sulfate). The suspension was filtered and concentrated under reduced pressure. The crude material was purified by silica gel chromatography eluting with 100% iso-hexane to 25% ethyl acetate in iso-hexane to afford the title compound (1.022 g, >100%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08877774B2 |
| 출처 데이터셋 | uspto-grants-2014_11 |
| ORD ID | ord-25d0f516749b4f2e97a0a4f49ecfd867 |
| 출처 메모 | uspto-grants-2014_11 |