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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1024757Erstellt: 25. Oktober 2026

Potassium Carbonate → 3-(2-Chloro-4-cyanophenoxy)-5-(4-cyanophenoxy)benzoic acid ethyl ester

https://huagongshe.com/reaction/1024757

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukt3-Chloro-4-fluorobenzonitrileHCID 145525—
Edukt3-(4-Cyanophenoxy)-5-hydroxy benzoic acid ethyl esterHCID 66818408—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-(2-Chloro-4-cyanophenoxy)-5-(4-cyanophenoxy)benzoic acid ethyl esterHCID 6681859779%

Reaktionsschritte

To 1.2 g (4.23 mmol) of 3-(4-cyano-phenoxy)-5-hydroxy-benzoic acid ethyl ester, dissolved in 10 ml of DMF, potassium carbonate 1.17 g (8.46 mmol) was added and stirred for 30 min at RT. 1.31 g (8.46 mmol) of 3-chloro-4-fluoro-benzonitrile, dissolved in 5 ml of DMF, was added dropwise to the reaction mixture during 15 min and final contents were stirred at 80° C. overnight. The reaction mixture was concentrated, residue was dissolved in 200 ml of ethyl acetate and partitioned with water. The organic layer was washed with brine followed by of water. Organic layer was dried over anhydrous sodium sulphate and concentrated under reduced pressure. The crude product was subjected to column chromatography, using silica-gel and eluted with hexane:ethyl acetate (8:2) to afford 1.4 g of pure product. 1H NMR (DMSO-d6): δ 1.3 (3H, t), 4.3 (2H, q), 7.2-7.36 (4H, m), 7.44 (2H, dd), 7.88 (3H, m), 8.26 (1H, d).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08722930B2
Quelldatensatzuspto-grants-2014_05
ORD IDord-96724c11222e4d60b344b7aa91a18f82
Quellennotizuspto-grants-2014_05