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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2164644Erstellt: 24. Oktober 2026

Chloroacetonitrile → (4-(4-(Methylsulfonyl)phenoxy)phenoxy)acetonitrile

https://huagongshe.com/de/reaction/2164644

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChloroacetonitrileHCID 7856—
EduktPotassium CarbonateHCID 11430—
EduktSodium HydroxideHCID 14798—
EduktPhenol, 4-(4-(methylsulfonyl)phenoxy)-HCID 514882—
LösungsmittelAcetonitrileHCID 6342—
Produkt(4-(4-(Methylsulfonyl)phenoxy)phenoxy)acetonitrileHCID 1307852092,4%

Reaktionsschritte

To a solution of 5.29 g (0.0200 mole) of 4-(4-(methylsulfonyl)phenoxy)phenol and 1.51 g (0.0200 mole) of 2-chloroacetonitrile in 100 ml of acetonitrile was added 3.0 g (0.0220 mole) of K2CO3. The mixture was heated at reflux for 3.5 hrs and cooled. The mixture was poured into aqueous NaOH and the product extracted from the mixture with CH2Cl2. The organic layer was extracted with aqueous NaOH, water and dried (Na2SO4). Removal of solvent in vacuo afforded 5.6 g (92.4% yield) of product. Recrystallization from ethanol followed by washing with aqueous NaOH and water afforded purified (4-(4-(methylsulfonyl)phenoxy)phenoxy)acetonitrile, mp 114°-115.5° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04505929
Quelldatensatzuspto-grants-1985_03
ORD IDord-36a243dff25145769df82ed4d451001c
Quellennotizuspto-grants-1985_03