Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 325227Erstellt: 25. Oktober 2026

Diethylamine → (4-Ethynyl-2-phenylbenzoyl)methionine methyl ester

https://huagongshe.com/reaction/325227

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethylamineHCID 8021—
EduktTrimethylsilylacetyleneHCID 66111—
EduktTetrabutylammonium FluorideHCID 2724141—
Edukt(2-Phenyl4bromobenzoyl)-methionine methyl esterHCID 20622824—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
KatalysatorPalladium(2+) acetate--triphenylphosphane (1/2/2)HCID 84538—
LösungsmittelTolueneHCID 1140—
LösungsmittelDiethyl EtherHCID 3283—
Produkt(4-Ethynyl-2-phenylbenzoyl)methionine methyl esterHCID 54338681—

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

A mixture of (2-phenyl-4-bromobenzoyl)-methionine methyl ester (100 mmol), diethylamine (300 mmol), trimethylsilylacetylene (110 mmol), bis(triphenylphosphine) palladium diacetate (5 mmol) and copper(I) iodide (3 mmol) in toluene is heated at 60° C. until TLC analysis indicates the starting methyl ester has disappeared. The reaction mixture is concentrated in vacuo, redissolved in ether, filtered through silica gel, and concentrated. The residue is then dissolved in THF, and is treated with tetrabutylammonium fluoride (120 mmol). After TLC analysis indicates that no starting material is left, the reaction mixture is diluted with ether, washed with water and brine, dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo. The residue is then purified with column chromatography on silica gel to give the title product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06221865B1
Quelldatensatzuspto-grants-2001_04
ORD IDord-b1295a32a5004ca08bcd2230412b11eb
Quellennotizuspto-grants-2001_04