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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 442708Erstellt: 24. Oktober 2026

Triphenylphosphine → 3-(3-Cyclopentyloxy-4-methoxyphenyl)-3-(3-nitrophenylethynyl)cyclohexan-1-one

https://huagongshe.com/de/reaction/442708

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriphenylphosphineHCID 11776—
Edukt1-Iodo-3-nitrobenzeneHCID 12574—
Edukt3-(3-Cyclopentyloxy-4-methoxyphenyl)-3-ethynylcyclohexan-1-oneHCID 15392007—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelTriethylamineHCID 8471—
Produkt3-(3-Cyclopentyloxy-4-methoxyphenyl)-3-(3-nitrophenylethynyl)cyclohexan-1-oneHCID 1585905790,1%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

To a solution of the compound from Example 3 (E1) (0.2 g, 0.64 mmol) and 3-iodonitrobenzene (Aldrich, 0.16 g, 0.64 mmol) in triethylamine (4 mL) under an argon atmosphere was added trace tetrakis(triphenylphosphine)palladium(0), copper(I) iodide and triphenylphosphine. The mixture was heated at 80° C. for 0.2 h, was cooled to room temperature and was concentrated in vacuo. The residue was partitioned between ethyl acetate and water. The organic phase was washed with brine, was dried (MgSO4) and was evaporated. Purification by flash chromatography, eluting with 3:1 hexanes/ethyl acetate, provided the title compound as yellow solid (0.25 g, 90%), m.p. 46°-48° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05891883
Quelldatensatzuspto-grants-1999_04
ORD IDord-98d4b94520ba4344b4e2e4dbea491123
Quellennotizuspto-grants-1999_04