HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
4-Ethynyl-1-(1-isopropoxycyclopropyl)-3-methyl-benzene → Ethyl4-[4-(1-isopropoxycyclopropyl)-3-methyl-phenylethynyl]-benzoate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 4-Ethynyl-1-(1-isopropoxycyclopropyl)-3-methyl-benzene | HCID 22568997 | — |
| Edukt | Ethyl-4-iodo-benzoate benzoate | HCID 69887287 | — |
| Katalysator | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Katalysator | HCID 178418476 | HCID 178418476 | — |
| Lösungsmittel | Triethylamine | HCID 8471 | — |
| Produkt | Ethyl4-[4-(1-isopropoxycyclopropyl)-3-methyl-phenylethynyl]-benzoate | HCID 22568844 | 159,2% |
Reaktionsschritte
Using General Procedure F; 4-ethynyl-1-(1-isopropoxycyclopropyl)-3-methyl-benzene (Intermediate 81, 80.0 mg, 0.13 mmol) and ethyl-4-iodo benzoate (Reagent A, 100.0 mg, 0.36 mmol) in triethylamine (5 mL) was treated with copper(I)iodide (25.0 mg, 0.13 mmol) and sparged with argon for 5 minutes. Dichlorobis(triphenylphosphine)-palladium(II) (91 mg, 0.13 mmol) was added and the reaction mixture was stirred overnight at room temperature. Column chromatography (2-4% EtOAc-hexanes) afforded 75.0 mg (56%) of the title compound as an orange solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06713647B2 |
| Quelldatensatz | uspto-grants-2004_03 |
| ORD ID | ord-8fadf66058e54861ba260ff04d8d7272 |
| Quellennotiz | uspto-grants-2004_03 |