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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1367921Erstellt: 25. Oktober 2026

Phenylacetylene → 6-Phenylethynyl-pyridine-2-carboxylic acid

https://huagongshe.com/reaction/1367921

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenylacetyleneHCID 10821—
Edukt6-Bromopyridine-2-carboxylic acidHCID 593919—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
KatalysatorHCID 178418476HCID 178418476—
LösungsmittelTriethylamineHCID 8471—
LösungsmittelSodium CarbonateHCID 10340—
Produkt6-Phenylethynyl-pyridine-2-carboxylic acidHCID 6694040493,3%

Reaktionsschritte

To a stirring solution 0.5 g (2.4 mmol) of 6-bromo-pyridine-2-carboxylic acid, 0.05 g (0.07 mmol) of dichlorobis(triphenylphosphine)-palladium(II), and 0.015 g (0.07 mmol) of copper (I) iodide in 10 mL of NEt3, 9.9 mL of 2 N Na2CO3 solution was added 0.38 g (3.7 mmol) of phenyl acetylene under nitrogen. After 12 h reflux under nitrogen, the reaction mixture was cooled and filtered. The filtrate was acidified using 2 N HCl (pH=5), and the resulting white precipitate was filtered, washed with water and dried to afford 0.5 g (51%) of 6-phenylethynyl-pyridine-2-carboxylic acid. LCMS: 224 (M+1)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07893267B2
Quelldatensatzuspto-grants-2011_02
ORD IDord-0e0608215b9d43b9989a3b2abdcea402
Quellennotizuspto-grants-2011_02