HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 29320Erstellt: 23. Oktober 2026
Tributylvinyltin → 3-Methyl-4-vinylbenzofuran-2-carboxylic acid ethyl ester
https://huagongshe.com/de/reaction/29320
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Tributylvinyltin | HCID 81998 | — |
| Edukt | Lithium Chloride | HCID 433294 | — |
| Edukt | 3-Methyl-4-trifluoromethanesulfonyloxy-benzofuran-2-carboxylic acid ethyl ester | HCID 86599026 | — |
| Katalysator | HCID 178418397 | HCID 178418397 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 3-Methyl-4-vinylbenzofuran-2-carboxylic acid ethyl ester | HCID 68713160 | 75,2% |
Reaktionsschritte
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.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07420001B2 |
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| Quelldatensatz | uspto-grants-2008_09 |
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| ORD ID | ord-b0c9cf25ebb547d1903fb5e5bb5ef8a5 |
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| Quellennotiz | uspto-grants-2008_09 |
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