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HRID 1107735Erstellt: 25. Oktober 2026

18-Crown-6 → 1-(2-Butenyl)-7-(4-fluorobenzyloxy)-2,3-dimethylpyrrolo[2,3-d]pyridazine

https://huagongshe.com/reaction/1107735

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt18-Crown-6HCID 28557—
Edukt4-Fluorobenzylic alcoholHCID 68022—
EduktPotassium tert-butoxideHCID 23665647—
Edukt1-(2-Butenyl)-7-chloro-2,3-dimethylpyrrolo[2,3-d]pyridazineHCID 53719624—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-(2-Butenyl)-7-(4-fluorobenzyloxy)-2,3-dimethylpyrrolo[2,3-d]pyridazineHCID 5399695463,1%

Reaktionsschritte

0.85 g (0.0076 mole) of potassium tert-butoxide was added to a solution of 0.48 g-(0.0038 mole) of 4-fluorobenzyl alcohol and 0.08 g (0.0003 mole) of 18-crown-6 in 30 ml of tetrahydrofuran and the mixture was stirred at room temperature for 10 minutes. 0.45 g (0.0019 mole) of 1-(2-butenyl)-7-chloro-2,3-dimethylpyrrolo[2,3-d]pyridazine was then added to the mixture and stirred at room temperature for 8 hours. After completion of the reaction, the reaction mixture was poured into ice-water and the aqueous mixture was extracted with dichloromethane. The extract was dried over anhydrous sodium sulfate and the solvent was distilled off under reduced pressure. The residue was purified by column chromatography through silica gel using a 4:1 mixture of toluene and ethyl acetate as an eluent. An oily material thus obtained was crystallized in hexane to give 0.39 g of 1-(2-butenyl)-7-(4-fluorobenzyloxy)-2,3-dimethylpyrrolo[2,3-d]pyridazine (cis/trans=13/87) as a pale brown powder.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06063782
Quelldatensatzuspto-grants-2000_05
ORD IDord-95641fdf7231455cac3415e881af0be1
Quellennotizuspto-grants-2000_05