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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164644Generated: October 26, 2026

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

https://huagongshe.com/reaction/2164644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetonitrileHCID 7856—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium HydroxideHCID 14798—
ReactantPhenol, 4-(4-(methylsulfonyl)phenoxy)-HCID 514882—
SolventAcetonitrileHCID 6342—
Product(4-(4-(Methylsulfonyl)phenoxy)phenoxy)acetonitrileHCID 1307852092.4%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04505929
Source datasetuspto-grants-1985_03
ORD IDord-36a243dff25145769df82ed4d451001c
Source noteuspto-grants-1985_03