Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Ethanone, 1-(3,5-bis(phenylmethoxy)phenyl)- → 1-(3,5-Bis(phenylmethoxy)phenyl)-2-bromoethan-1-one
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Ethanone, 1-(3,5-bis(phenylmethoxy)phenyl)- | HCID 120098 | — |
| 반응물 | Tetra-n-butylammonium tribromide | HCID 23500184 | — |
| 용매 | Methanol | HCID 887 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1-(3,5-Bis(phenylmethoxy)phenyl)-2-bromoethan-1-one | HCID 120097 | — |
반응 단계
To a stirred solution of 1-[3,5-bis(benzyloxy)phenyl]ethanone (5 g, 15.04 mmol) in tetrahydrofuran (60 mL) and methanol (35 mL) was added tetrabutylammonium tribromide (7.25 g, 15.04 mmol) in tetrahydrofuran (20 mL) at room temperature. The reaction mixture was stirred for 24 hours and the solvent removed in vacuo. The residue was dissolved in ethyl acetate (100 mL) and washed with water (2×50 mL). The combined organic extracts were dried over magnesium sulfate and concentrated to afford the desired compound as a yellow oil in quantitative yield.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07538141B2 |
| 출처 데이터셋 | uspto-grants-2009_05 |
| ORD ID | ord-37b82bc9545047b0916a4cec67c3ded1 |
| 출처 메모 | uspto-grants-2009_05 |