참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Tributylvinyltin | HCID 81998 | — |
| 반응물 | Lithium Chloride | HCID 433294 | — |
| 반응물 | 3-Methyl-4-trifluoromethanesulfonyloxy-benzofuran-2-carboxylic acid ethyl ester | HCID 86599026 | — |
| 촉매 | HCID 178418397 | HCID 178418397 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 3-Methyl-4-vinylbenzofuran-2-carboxylic acid ethyl ester | HCID 68713160 | 75.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07420001B2 |
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| 출처 데이터셋 | uspto-grants-2008_09 |
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| ORD ID | ord-b0c9cf25ebb547d1903fb5e5bb5ef8a5 |
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| 출처 메모 | uspto-grants-2008_09 |
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