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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 37102Erstellt: 24. Oktober 2026

Phenol → HCID 19934777, Verbindung

https://huagongshe.com/de/reaction/37102

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenolHCID 996—
EduktSodium HydroxideHCID 14798—
EduktPhenolate SodiumHCID 4445035—
Edukt4-tert-butyl-N-[5-(2-chloro-5-methoxy-phenoxy)-6-chloromethyl-2-(morpholin-4-yl)-pyrimidin-4-yl]-benzenesulphonamideHCID 19934755—
LösungsmittelAcetoneHCID 180—
LösungsmittelWaterHCID 962—
ProduktHCID 19934777HCID 19934777—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

0.145 g of 4-tert.-butyl-N-[5-(2-chloro-5-methoxy-phenoxy)-6-chloromethyl-2-(morpholin-4-yl)-pyrimidin-4-yl]benzenesulphonamide (Example 4) in 3 ml of acetone was added to a sodium phenolate solution from 0,024 g of phenol and 0.06 g of NaOH in 2 ml of acetone and 1 ml of water. The reaction mixture was stirred at 80° C. under argon for 48 hours. Thereafter, the acetone was distilled off and the residue was partitioned between chloroform and water. The chloroform phase was washed with water, dried over sodium sulphate and the solvent was distilled off. The residue was chromatographed over silica gel with chloroform. 0.07 g of 4-tert.-butyl-N-[5-(2-chloro-5-methoxy-phenoxy)-2-morpholin-4-yl-6-phenoxymethyl-pyrimidin-4-yl]benzenesulphonamide, MS: M=639, was obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05420129
Quelldatensatzuspto-grants-1995_05
ORD IDord-d0aa28ba710c4f8cadc523ef1d3f73ae
Quellennotizuspto-grants-1995_05