HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 224Erstellt: 24. Oktober 2026
1-Phenethylpiperazine → 1-Benzofuran-7-yl-4-phenethyl-piperazine; hydrochloride
https://huagongshe.com/de/reaction/224
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1-Phenethylpiperazine | HCID 79214 | — |
| Edukt | 7-Bromo-1-benzofuran | HCID 113628 | — |
| Reagenz | Sodium t-butoxide | HCID 23676156 | — |
| Katalysator | Binap, (A+-)- | HCID 634876 | — |
| Katalysator | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 1-Benzofuran-7-yl-4-phenethyl-piperazine; hydrochloride | HCID 10018047 | 62,12% |
Reaktionsschritte
A dried Radley tube was charged with rac-2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl (6.32 mg, 10.15 µmol), Tris(dibenzylideneacetone)dipalladium(0) (4.65 mg, 5.08 µmol) and Sodium tert- butoxide (34.1 mg, 0.36 mmol). Argon atmosphere was introduced and toluene (3ml) was added followed by 7-bromobenzofuran (50mg, 0.25 mmol) and 1-phenethylpiperazine (48.3 mg, 0.25 mmol). The reaction mixture was heated at reflux over night. 2010-03-25 The reaction mixture was filtered, concentrated and purified by flash chromatography (Isolute Si 10g, heptane: ethyl acetate; 4:1) to give 1-(benzofuran-7-yl)-4-phenethylpiperazine (48.3 mg, 62.1 %)
Herkunft & Nachweise
| Quelldatensatz | 750 AstraZeneca ELN dataset |
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| ORD ID | ord-8cfc6888cfb048a3bbd7a788345f4499 |
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| Quellennotiz | 750 AstraZeneca ELN dataset |
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