Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Tetrahydrofuran → 3-Bromo-2-methyl-5-[3-(trifluoromethyl)phenyl]thiophene
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | Cesium carbonate | HCID 10796 | — |
| 반응물 | 3,5-Dibromo-2-methylthiophene | HCID 122373 | — |
| 반응물 | 3-(Trifluoromethyl)phenylboronic acid | HCID 2734388 | — |
| 촉매 | HCID 178418397 | HCID 178418397 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 3-Bromo-2-methyl-5-[3-(trifluoromethyl)phenyl]thiophene | HCID 66939431 | 85.7% |
반응 단계
Under a nitrogen atmosphere, a mixture of 3,5-dibromo-2-methylthiophene (2.00 g), 3-(trifluoromethyl)phenylboronic acid (2.23 g), tetrakis(triphenylphosphine)palladium (0.45 g), cesium carbonate (5.09 g) and tetrahydrofuran (40 mL) was heated under reflux for 16 hr. The reaction mixture was cooled, water was added, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by column chromatography (carrier: silica gel, eluent: hexane-ethyl acetate) to give the title compound (2.15 g) as a solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08461348B2 |
| 출처 데이터셋 | uspto-grants-2013_06 |
| ORD ID | ord-99d89984852d4b4d9147b9157afb8d38 |
| 출처 메모 | uspto-grants-2013_06 |