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HRID 2760Erstellt: 23. Oktober 2026

Tributylamine → 4H,5H-thieno(3,2-c)pyridin-4-one

https://huagongshe.com/de/reaction/2760

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTributylamineHCID 7622—
EduktTriethylamineHCID 8471—
EduktEthyl chloroformateHCID 10928—
EduktSodium AzideHCID 33557—
Edukt3-Thiophen-2-ylprop-2-enoic acidHCID 92868—
LösungsmittelAcetoneHCID 180—
LösungsmittelWaterHCID 962—
LösungsmittelDiphenyl EtherHCID 7583—
Produkt4H,5H-thieno(3,2-c)pyridin-4-oneHCID 28852549,7%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of 3-thiophene-2-yl-acrylic acid (7.39 g, 47.9 mmol) in 200 mL of acetone is added triethylamine (4.9 g, 47.9 mmol). The resulting solution is cooled to 0° C. and ethyl chloroformate (5.7 g, 52.8 mmol) is added dropwise. After 2 h, sodium azide (4.67 g, 71.9 mmol) in 25 mL of H2O is then added. The solution is stirred for 1.5 h at 0° C. After this time, the solution is poured into 300 mL of H2O. A white precipitate forms which is collected by filtration. The resulting solid is dried over P2O5 under vacuum. The solid is suspended in 20 mL of diphenyl ether. This solution is added dropwise to a solution of tributylamine (6.9 g, 37.4 mmol) in 200 ml of diphenyl ether at 190° C. After 2 h, the solution is cooled to ambient temperatures. The solution is diluted with 1000 mL of hexanes and is cooled to 0° C. The resulting solid is collected by filtration and the solid is washed with hexanes. The title compound (3.6 g, 23.8 mmol) is obtained as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05731315
Quelldatensatzuspto-grants-1998_03
ORD IDord-1904bdb207a945399ea4b67f6fd8eb2b
Quellennotizuspto-grants-1998_03