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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29320생성일: 2026년 10월 24일

Tributylvinyltin → 3-Methyl-4-vinylbenzofuran-2-carboxylic acid ethyl ester

https://huagongshe.com/ko/reaction/29320

반응식

참여 물질

역할이름HCID투입량
반응물TributylvinyltinHCID 81998—
반응물Lithium ChlorideHCID 433294—
반응물3-Methyl-4-trifluoromethanesulfonyloxy-benzofuran-2-carboxylic acid ethyl esterHCID 86599026—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물3-Methyl-4-vinylbenzofuran-2-carboxylic acid ethyl esterHCID 6871316075.2%

반응 조건

온도90 °C

반응 단계

To a solution of 2.48 g (7.05 mmol) of 3-methyl-4-trifluoromethanesulfonyloxy-benzofuran-2-carboxylic acid ethyl ester (Example 20, Step 2) in 30 mL of DMF was added 2.16 mL (7.40 mmol) of vinyl tributyltin, 0.898 g (21.1 mmol) of lithium chloride and 0.247 g (0.352 mmol) of tetrakis(triphenylphosphine)palladium(0). The reaction was heated to 90° C. for 3 h and then cooled to room temperature. The reaction was diluted with water and extracted with ether. The combined organics were washed with water and brine, dried over magnesium sulfate, filtered and concentrated in vacuo. The residue was chromatographed on silica gel eluting with ethyl acetate/hexanes (1:25) to provide 1.22 g of 3-methyl-4-vinylbenzofuran-2-carboxylic acid ethyl ester.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07420001B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-b0c9cf25ebb547d1903fb5e5bb5ef8a5
출처 메모uspto-grants-2008_09