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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 28460생성일: 2026년 10월 26일

(R)-[8-allyl-7-nitro-2,3-dihydro-1,4-benzodioxin-2-yl]methyl4-methylbenzenesulfonate → {7-Nitro-8-[1-propenyl]-2,3-dihydro-1,4-benzodioxin-2-yl}methyl 4-methylbenzenesulfonate

https://huagongshe.com/reaction/28460

반응식

참여 물질

역할이름HCID투입량
반응물(R)-[8-allyl-7-nitro-2,3-dihydro-1,4-benzodioxin-2-yl]methyl4-methylbenzenesulfonateHCID 12082206—
촉매Bis(acetonitrile)dichloropalladiumHCID 6093782—
용매BenzeneHCID 241—
생성물{7-Nitro-8-[1-propenyl]-2,3-dihydro-1,4-benzodioxin-2-yl}methyl 4-methylbenzenesulfonateHCID 7385242274%

반응 단계

To a solution of 10.0 g (24.0 mmole) of (R)-[8-allyl-7-nitro-2,3-dihydro-1,4-benzodioxin-2-yl]methyl 4-methylbenzenesulfonate in 700 mL of benzene was added 1.03 g of bis(acetonitrile)dichloropalladium (II) and the mixture was refluxed under nitrogen for 48 hours. The catalyst was then removed by filtration, and the filtrate concentrated in vacuum to a brown oil. Column chromatography on silica gel with methylene chloride as eluent gave 7.2 g of the title compound as a mixture of E and Z isomers. A sample of {(2R)-7-nitro-8[(E)-1-propenyl]-2,3-dihydro-1,4-benzodioxin-2-yl}methyl 4-methylbenzenesulfonate was obtained as a yellow solid (m.p. 105-106° C.) by evaporation of a pure E isomer-containing fraction.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07419986B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-2af5cb9668e24167990e36f06d087d65
출처 메모uspto-grants-2008_09