HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 351428Erstellt: 25. Oktober 2026
Potassium Hydroxide → 4'-Benzyloxyphenyl acetylene
https://huagongshe.com/reaction/351428
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | Trimethylsilylacetylene | HCID 66111 | — |
| Edukt | 1-(Benzyloxy)-4-iodobenzene | HCID 519671 | — |
| Katalysator | HCID 178418476 | HCID 178418476 | — |
| Lösungsmittel | Diethylamine | HCID 8021 | — |
| Produkt | 4'-Benzyloxyphenyl acetylene | HCID 1490323 | — |
Reaktionsschritte
4-benzyloxy iodobenzene (193 g, 0.625 mol), ethynyl-trimethyl-silane (75 g, 0.76 mol), Cul (2 g, 10.5 mmol) and Pd(PPh3)2Cl2 (1 g, 1.0 mmol) were added to diethylamine (880 mL) at 0° C. The reaction mixture was warmed to 25° C. and then stirred for 6 h. The reaction mixture was concentrated and partitioned in H2O/ethyl acetate (100 mL/100 mL). The reaction mixture was further extracted with ethyl acetate (300 mL×2). The combined organic layers were washed by water (300 mL), dried over MgSO4 and concentrated in vacuo. The crude product was dissolved in methanol (400 mL) and was stirred with KOH (28 g, 0.5 mol) for 1 h at 25° C. Concentration and purification by silica gel column chromatograph (5% ethyl acetate/Hexane) yielded 4-benzyloxy phenyl acetylene as liquid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07183445B2 |
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| Quelldatensatz | uspto-grants-2007_02 |
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| ORD ID | ord-7f0bafc984b14b18824e44153f5ddef6 |
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| Quellennotiz | uspto-grants-2007_02 |
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