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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 7760Erstellt: 24. Oktober 2026

Ethyl Acetate → 5-(1,3-Benzoxazol-2-yl)-2-pyridin-2-yl benzonitrile

https://huagongshe.com/de/reaction/7760

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
Edukt2-(Tributylstannyl)pyridineHCID 607784—
Edukt4-(1,3-Benzoxazol-2-yl)-2-cyanophenyl trifluoromethanesulfonateHCID 21990967—
KatalysatorHCID 178418397HCID 178418397—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
LösungsmittelSodium chloride; waterHCID 57417360—
Produkt5-(1,3-Benzoxazol-2-yl)-2-pyridin-2-yl benzonitrileHCID 10236467—

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

The degassed solution of 4-(1,3-benzoxazol-2-yl)-2-cyanophenyl trifluoromethanesulfonate (300 mg, 1.2 mmol) in DME (5 mL) was added 2-tri-n-butylstannylpyridine (273 mg, 0.74 mmol), tetrakis(triphenylphosphine)palladium(0) (150 mg, 0.1 mmol). The reaction was stirred at 90° C. overnight and cooled to rt. EtOAc (100 mL) was added, as well as brine (50 mL). The organic layer was washed with brine (2×20 mL), dried (MgSO4), and the crude material was purified on flash column (silica gel, hexanes:EtOAc 3:1) to afford desired 5-(1,3-benzoxazol-2-yl)-2-pyridin-2-yl benzonitrile as pinkish solid. 1H NMR (CD3OD, 300 MHz), δ 8.85 (d 1H), 8.72 (d, 1H), 8.59 (m, 1H), 8.08 (d, 1H), 7.91 (d, 2H), 7.85 (m, 1H), 7.65 (m, 1H), 7.45 (m, 3H). MS (ESI) 298 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07087601B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-2b86ba7fc6984a3c8299ef5961aa3279
Quellennotizuspto-grants-2006_08