Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Tributylstannane → 1-Fluoro-3-(4-chlorophenyl)-3-methyl-1-tributylstannyl-1-butene
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Tributylstannane | HCID 5948 | — |
| 반응물 | Azobisisobutyronitrile | HCID 6547 | — |
| 반응물 | 1-Fluoro-1-phenylsulfonyl-3-methyl-3-(4-chlorophenyl)-1-butene | HCID 53860513 | — |
| 용매 | Cyclohexane | HCID 8078 | — |
| 생성물 | 1-Fluoro-3-(4-chlorophenyl)-3-methyl-1-tributylstannyl-1-butene | HCID 67632345 | — |
반응 단계
Under a nitrogen atmosphere, a stirring solution of 22.7 grams (0.067 mole) of 1-fluoro-1-phenylsulfonyl-3-methyl-3-(4-chlorophenyl)-1-butene, 42.0 grams (0.14 mole) of tributyltin hydride, and 0.5 gram (catalyst) of azobisisobutyronitrile in 700 mL of cyclohexane is heated at reflux for about three hours. After this time the reaction mixture is cooled to ambient temperature, and 125 mL of silica gel is added. The mixture is concentrated under reduced pressure, and the residue is subjected to column chromatography. The product-containing fractions are combined and concentrated under reduced pressure, yielding 1-fluoro-3-(4-chlorophenyl)-3-methyl-1-tributylstannyl-1-butene.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05622954 |
| 출처 데이터셋 | uspto-grants-1997_04 |
| ORD ID | ord-beee978054c2486f921e37cce4ee1d7b |
| 출처 메모 | uspto-grants-1997_04 |