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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 54267생성일: 2026년 10월 25일

Tributylstannane → 1-Fluoro-3-(4-chlorophenyl)-3-methyl-1-tributylstannyl-1-butene

https://huagongshe.com/reaction/54267

반응식

참여 물질

역할이름HCID투입량
반응물TributylstannaneHCID 5948—
반응물AzobisisobutyronitrileHCID 6547—
반응물1-Fluoro-1-phenylsulfonyl-3-methyl-3-(4-chlorophenyl)-1-buteneHCID 53860513—
용매CyclohexaneHCID 8078—
생성물1-Fluoro-3-(4-chlorophenyl)-3-methyl-1-tributylstannyl-1-buteneHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05622954
출처 데이터셋uspto-grants-1997_04
ORD IDord-beee978054c2486f921e37cce4ee1d7b
출처 메모uspto-grants-1997_04