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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 351428Erstellt: 25. Oktober 2026

Potassium Hydroxide → 4'-Benzyloxyphenyl acetylene

https://huagongshe.com/reaction/351428

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium HydroxideHCID 14797—
EduktTrimethylsilylacetyleneHCID 66111—
Edukt1-(Benzyloxy)-4-iodobenzeneHCID 519671—
KatalysatorHCID 178418476HCID 178418476—
LösungsmittelDiethylamineHCID 8021—
Produkt4'-Benzyloxyphenyl acetyleneHCID 1490323—

Reaktionsbedingungen

Temperatur25 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07183445B2
Quelldatensatzuspto-grants-2007_02
ORD IDord-7f0bafc984b14b18824e44153f5ddef6
Quellennotizuspto-grants-2007_02