HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 602069Erstellt: 25. Oktober 2026
1-Bromo-3,5-dimethoxybenzene → 3-(3,5-Dimethoxyphenyl)-1-propene
https://huagongshe.com/reaction/602069
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1-Bromo-3,5-dimethoxybenzene | HCID 639187 | — |
| Edukt | 4,4,5,5-Tetramethyl-2-(prop-2-en-1-yl)-1,3,2-dioxaborolane | HCID 2763171 | — |
| Katalysator | Palladium | HCID 23938 | — |
| Produkt | 3-(3,5-Dimethoxyphenyl)-1-propene | HCID 524874 | — |
Reaktionsschritte
The Pd-catalyzed cross-coupling reaction of 5-Bromo-1,3-dimethoxybenzene with allyl boronic acid pinacol ester produced 5-allyl-1,3-dimethoxybenzene 1 in excellent yield. AlI3 will be used for demethylating 5-Allyl-1,3-dimethoxybenzene with CS2 as solvent to produce 5-allylresorcinol 2. The bis(phosphinite) PCP ligands 3 will be obtained by diphosphorylation of 5-allylresorcinol 2 with the respective chlorophosphine and sodium hydride as a base. Iridium complexes 4 will be obtained from reaction of the respective PCP ligands 3 with [Ir(COD)Cl]2 or [Ir(COE)2Cl]2. Hydrosilylation of complexes 4 will produce the hydrosilylated complexes 5. Reaction of complexes 5 with silica gel will afford the Si2O-supported Ir complexes 6. To date, 5-allyl-1,3-dimethoxybenzene 1 has been prepared in 92% yield.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07902417B2 |
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| Quelldatensatz | uspto-grants-2011_03 |
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| ORD ID | ord-376ca710da7348ff836753aa74e52718 |
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| Quellennotiz | uspto-grants-2011_03 |
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