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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 594109Erstellt: 26. Oktober 2026

Cesium carbonate → 6-Ethenyl-2-methyl-3-nitropyridine

https://huagongshe.com/reaction/594109

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCesium carbonateHCID 10796—
Edukt2-Ethenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 5233012—
Edukt6-Bromo-2-methyl-3-nitropyridineHCID 24728014—
Katalysatorpalladium(II) acetateHCID 167845—
Katalysator2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
LösungsmittelWaterHCID 962—
Lösungsmittel2-MethyltetrahydrofuranHCID 7301—
Produkt6-Ethenyl-2-methyl-3-nitropyridineHCID 68452810116,3%

Reaktionsschritte

A suspension/solution of 6-bromo-2-methyl-3-nitropyridine (500 mg, 2.304 mmol), 2-ethenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (0.782 mL, 4.61 mmol), palladium(II) acetate (25.9 mg, 0.115 mmol), X-phos (110 mg, 0.230 mmol) and cesium carbonate (3.0 g, 9.22 mmol) in 2-methyltetrahydrofuran (2-MeTHF) (8 mL) and water (2 mL) was stirred under nitrogen at 60° C. for 1 hour. The reaction mixture was cooled then separated between ethyl acetate and water. The organic phase was washed with brine and dried over magnesium sulphate. The solvent was removed in vacuo and the residue was dissolved in DCM (5 mL). This was applied to a silica cartridge and eluted with a gradient of 0-100% ethyl acetate in cyclohexane. This gave the crude product (440 mg) as a brown liquid which was used directly in the next step with no further purification. LCMS (2 min, formic) Rt 0.91 min, m/z (ES+) 165 (M+H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09242972B2
Quelldatensatzuspto-grants-2016_01
ORD IDord-a54ef7cd6cc04d60a0c52759cf1efeea
Quellennotizuspto-grants-2016_01