HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 927122Erstellt: 26. Oktober 2026
4-Bromo-2-methyl-1-(trifluoromethyl)benzene → 3,4-Bis(benzyloxy)-6-((3-methyl-4-(trifluoromethyl)phenyl)-ethynyl)pyridazine
https://huagongshe.com/reaction/927122
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-Bromo-2-methyl-1-(trifluoromethyl)benzene | HCID 45790478 | — |
| Edukt | 3,4-Bis(benzyloxy)-6-ethynylpyridazine | HCID 86677025 | — |
| Edukt | 1,8-Diazabicycloundec-7ene | HCID 129662960 | — |
| Katalysator | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Katalysator | HCID 178418476 | HCID 178418476 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 3,4-Bis(benzyloxy)-6-((3-methyl-4-(trifluoromethyl)phenyl)-ethynyl)pyridazine | HCID 71269897 | 27,1% |
Reaktionsschritte
3,4-bis(Benzyloxy)-6-ethynylpyridazine (Intermediate 5; 3.0 g, 9.48 mmol), copper(I) iodide (0.181 g, 0.948 mmol) and bis(triphenylphosphine)-palladium(II) dichloride (0.333 g, 0.474 mmol) were combined. The reaction vessel was purged with nitrogen, followed by the addition of 4-bromo-2-methyl-1-(trifluoromethyl)benzene (2.493 g, 10.43 mmol), 1,8-diazabicycloundec-7-ene (8.66 g, 56.9 mmol) and tetrahydrofuran (32 ml) before the resulting mixture was allowed to stir at room temperature overnight. The reaction was quenched with brine and extracted into ethyl acetate (×2) and the combined organic extracts were washed with brine, dried (MgSO4) and concentrated in vacuo to afford a dark brown gum. The gum was purified by column chromatography (silica, 0-50% ethyl acetate in petrol) to afford 3,4-bis(benzyloxy)-6-((3-methyl-4-(trifluoromethyl)phenyl)-ethynyl)pyridazine as a dark brown oil (1.22 g, 27%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09290456B2 |
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| Quelldatensatz | uspto-grants-2016_03 |
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| ORD ID | ord-594ce1e37bab4f0a90d50822147e048c |
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| Quellennotiz | uspto-grants-2016_03 |
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