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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 76177Erstellt: 24. Oktober 2026

3-Ethynylbenzoic acid methyl ester → Methyl 3-((4-(2-acetamidopropyl)phenyl)ethynyl)benzoate

https://huagongshe.com/de/reaction/76177

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Ethynylbenzoic acid methyl esterHCID 11275159—
EduktN-(1-(4-Iodophenyl)propan-2-YL)acetamideHCID 66611344—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
KatalysatorDichlorobis(triphenylphosphine)palladiumHCID 6102075—
LösungsmittelDimethylformamideHCID 6228—
ProduktMethyl 3-((4-(2-acetamidopropyl)phenyl)ethynyl)benzoateHCID 66611163—

Reaktionsschritte

To 10.0 g (63.4 mmol) methyl 3-ethynylbenzoate (J. Org. Chem. 1981, 46, 2280-6) and 7.00 g (23.1 mmol) N-(1-(4-iodo-phenyl)propan-2-yl)acetamide (I52.1) in 80 mL DMF are added 100 mL TEA, 250 mg (1.31 mmol) CuI and 1.20 g (1.71 mmol) bis(triphenylphosphine)-palladium (II) chloride. After stirring over night r.t. the solvents are removed under reduced pressure. The residue is partitioned between EtOAc and diluted aq. NH4Cl solution. The organic layer is separated and the aq. layer is extracted with EtOAc (2×). The org. layers are combined, washed with brine, dried with Na2SO4 and the solvent is removed in vacuo. The residue is purified by column chromatography (silica gel, EtOAc 100%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08835472B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-80a171854e3a4cd182eb4751a6186526
Quellennotizuspto-grants-2014_09