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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTributylvinyltinHCID 81998—
EduktLithium ChlorideHCID 433294—
Edukt3-Methyl-4-trifluoromethanesulfonyloxy-benzofuran-2-carboxylic acid ethyl esterHCID 86599026—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-Methyl-4-vinylbenzofuran-2-carboxylic acid ethyl esterHCID 6871316075,2%

Reaktionsbedingungen

Temperatur90 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07420001B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-b0c9cf25ebb547d1903fb5e5bb5ef8a5
Quellennotizuspto-grants-2008_09