HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 18-Crown-6 | HCID 28557 | — |
| Edukt | 4-Fluorobenzylic alcohol | HCID 68022 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Edukt | 1-(2-Butenyl)-7-chloro-2,3-dimethylpyrrolo[2,3-d]pyridazine | HCID 53719624 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 1-(2-Butenyl)-7-(4-fluorobenzyloxy)-2,3-dimethylpyrrolo[2,3-d]pyridazine | HCID 53996954 | 63,1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06063782 |
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| Quelldatensatz | uspto-grants-2000_05 |
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| ORD ID | ord-95641fdf7231455cac3415e881af0be1 |
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| Quellennotiz | uspto-grants-2000_05 |
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