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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 897465Erstellt: 23. Oktober 2026

Water → 5-Bromo-2-phenoxypyrimidine

https://huagongshe.com/de/reaction/897465

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktPhenolHCID 996—
EduktPotassium HydroxideHCID 14797—
Edukt5-Bromo-2-chloropyrimidineHCID 606665—
KatalysatorDibenzo-18-crown-6HCID 26541—
LösungsmittelTolueneHCID 1140—
Produkt5-Bromo-2-phenoxypyrimidineHCID 64284254,4%

Reaktionsschritte

A mixture of 5-bromo-2-chloropyrimidine (5.00 g, 0.0259 mol), phenol (3.16 g, 0.0336 mol), dibenzo-18-Crown-6 (0.47 g, 0.0013 mol) and ground potassium hydroxide (3.51 g, 0.0626 mol) in toluene (75 ml) was heated at reflux for 5 hours with azeotropic removal of water. The mixture was allowed to cool to ambient temperature and the solvent was removed under reduced pressure. The residue was partitioned between water and chloroform. The layers were separated and the aqueous phase was extracted with chloroform three times. The combined organic layers were dried over magnesium sulfate, filtered and evaporated. The residue was purified by flash column chromatography on silica using n-heptane/ethyl acetate (98:2) as an eluent to give 5-bromo-2-phenoxy-pyrimidine as a white solid (3.55 g, 0.0141 mol): 1H NMR (DMSO-d6, 400 MHz) 8.80 (s, 2H), 7.45 (t, 2H), 7.27 (t, 1H), 7.22 (d 2H); TLC (n-heptane/ethyl acetate=95:5) Rf 0.20.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06921763B2
Quelldatensatzuspto-grants-2005_07
ORD IDord-ece28418e4614288bf5fd0fd7c32b5ee
Quellennotizuspto-grants-2005_07