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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 39291Erstellt: 24. Oktober 2026

Triethylamine → 5-(3,3-Dimethyl-but-1-ynyl)-thiophene-2-carboxylic acid ethyl ester

https://huagongshe.com/de/reaction/39291

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt3,3-Dimethyl-1-butyneHCID 13512—
EduktEthyl 5-bromothiophene-2-carboxylateHCID 605723—
KatalysatorCopper iodideHCID 83717—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
LösungsmittelDimethylformamideHCID 6228—
Produkt5-(3,3-Dimethyl-but-1-ynyl)-thiophene-2-carboxylic acid ethyl esterHCID 5811412897,3%

Reaktionsschritte

A mixture of 5-Bromo-thiophene-2-carboxylic acid ethyl ester (7 g, 30 mmol), copper iodide (1.2 g, 6 mmol), triethylamine (20 mL) in DMF (100 mL) was degassed in a 350 mL pressure bottle. Then tris(dibenzylideneacetone)dipalladium(0) (2.1 g, 3 mmol) and 3,3-dimethyl-but-1-yne (18.3 mL, 150 mmol) were added and heated at 80 degree for 3 hours. The reaction mixture was filtered on celite and washed with ethyl acetate. The solution was diluted with water and extracted twice with ethyl acetate. The organic phases were combined and washed with water. After drying and concentration, the crude residue was purified by flash chromatography to yield 6.9 g (95%) of 5-(3,3-Dimethyl-but-1-ynyl)-thiophene-2-carboxylic acid ethyl ester as a yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524764B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-32d5be6c632a4182b5049936e8f684b9
Quellennotizuspto-grants-2013_09