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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1756174Erstellt: 26. Oktober 2026

Water → (E)-N-ethyl-N-(2-penten-4-ynyl)-2-[2-[3-(3-thienyl)phenoxy]ethoxy]ethylamine

https://huagongshe.com/reaction/1756174

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktEthyl AcetateHCID 8857—
Edukt(E)-N-ethyl-N-(5-trimethylsilyl-2-penten-4-ynyl)-2-[2-[3-(3-thienyl)phenoxy]ethoxy]ethylamineHCID 19917013—
LösungsmittelMethanolHCID 887—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelPotassium FluorideHCID 522689—
Produkt(E)-N-ethyl-N-(2-penten-4-ynyl)-2-[2-[3-(3-thienyl)phenoxy]ethoxy]ethylamineHCID 1991704178,2%

Reaktionsschritte

2.0 g of the resulting allylamine compound was dissolved in a mixture of methanol (5 ml) and tetrahydrofuran (5 ml), and 10 ml of a saturated aqueous solution of potassium fluoride was added. The mixture was stirred overnight at room temperature, and then ethyl acetate and water were added. The organic layer separated was worked up in a customary manner, and the product was purified by silica gel column chromatography [methylene chloride/methanol=100/1] to give 1.3 g of (E)-N-ethyl-N-(2-penten-4-ynyl)-2-[2-[3-(3-thienyl)phenoxy]ethoxy]ethylamine as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05439932
Quelldatensatzuspto-grants-1995_08
ORD IDord-d22b8a90a9b6490289afc8a4116b7dcf
Quellennotizuspto-grants-1995_08