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HRID 220157Erstellt: 26. Oktober 2026

Potassium Phosphate, Tribasic → Methyl 6-(1,4-dioxaspiro[4,5]dec-7-en-8-yl)nicotinate

https://huagongshe.com/reaction/220157

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium Phosphate, TribasicHCID 62657—
Edukt2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
EduktMethyl 6-bromopyridine-3-carboxylateHCID 13349623—
Edukt1,4-Dioxaspiro[4.5]dec-7-en-8-ylboronic acidHCID 44118765—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelWaterHCID 962—
Lösungsmittel1,4-DioxaneHCID 31275—
ProduktMethyl 6-(1,4-dioxaspiro[4,5]dec-7-en-8-yl)nicotinateHCID 69059497—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

Methyl 6-bromonicotinate (2.11 g, 9.78 mmol), 1,4-dioxaspiro[4,5]dec-7-en-8-ylboronic acid (2 g, 10.86 mmol), palladium(II) acetate (109 mg, 0.48 mmol), dicyclohexyl(2′,6′-dimethoxybiphenyl-2-yl)phosphine (0.40 g, 0.97 mmol) and potassium phosphate (6.2 g, 29.1 mmol) were placed in a Schlenk tube and the tube was placed under vacuum and filled with argon. Dioxane (30 mL) and water (4 mL) were added and the tube was heated (80° C.) overnight. The mixture was partitioned with ether and water and the organic phase was washed with brine, dried (magnesium sulfate), filtered and evaporated. The residue was purified by silica gel chromatography using 30% ethyl acetate in hexanes to provide the title compound as a slightly yellow oil, which solidified upon standing.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08202878B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-909c7d57072e4cd282d7957ed33929fd
Quellennotizuspto-grants-2012_06