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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 351536Erstellt: 25. Oktober 2026

Ethyl 4-bromobenzoate → Ethyl 4-(4-n-pentyloxyphenylethynyl)benzoate

https://huagongshe.com/reaction/351536

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl 4-bromobenzoateHCID 22043—
Edukt1-Eth-1-ynyl-4-(pentyloxy)benzeneHCID 2775119—
KatalysatorTriphenylphosphineHCID 11776—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
KatalysatorDichlorobis(triphenylphosphine)palladiumHCID 6102075—
LösungsmittelPyridineHCID 1049—
LösungsmittelTriethylamineHCID 8471—
ProduktEthyl 4-(4-n-pentyloxyphenylethynyl)benzoateHCID 2271325935,2%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

To a suspension of ethyl 4-bromobenzoate (1.37 g), (4-n-pentyloxyphenyl)acetylene (565 mg), triphenylphosphine (16 mg) and copper(I) iodide (6 mg) in triethylamine (10 ml) and pyridine (4 ml) was added palladium(II) chloride bis(triphenylphosphine) (21 mg) and the reaction mixture was stirred for 24 hours at 80° C. After cooling, the precipitate was filtered off, and the filtrate was evaporated under reduced pressure. The residue was taken up to dichloromethane, and the solution was washed successively with 1N HCl, water, brine and dried over magnesium sulfate. The solvents were removed under reduced pressure and the residue was triturated with acetonitrile, collected by filtration and dried under reduced pressure to give ethyl 4-(4-n-pentyloxyphenylethynyl)benzoate (355 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06743776B2
Quelldatensatzuspto-grants-2004_06
ORD IDord-75df36affa3b4e1c9e154e2606ab4cdf
Quellennotizuspto-grants-2004_06