Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515154Generated: October 29, 2026

Morpholine → 2-(Ethylsulfonyl)-6-methyl-4-morpholin-4-yl-benzonitrile

https://huagongshe.com/reaction/515154

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Chloro-2-(ethylsulfonyl)-6-methyl-benzonitrileHCID 86699731—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product2-(Ethylsulfonyl)-6-methyl-4-morpholin-4-yl-benzonitrileHCID 8669973096%

Reaction Conditions

Temperature150 °C

Reaction Steps

4-Chloro-2-(ethylsulfonyl)-6-methyl-benzonitrile (0.43 g, 1.77 mmol), morpholine (0.46 ml, 5.31 mmol) and potassium carbonate (0.32 g, 2.30 mmol) are taken up in N-methyl-2-pyrrolidone (3 ml) in a sealed tube and the resulting mixture is heated at 150° C. for 2 d. The mixture is then diluted with water (6 ml) and extracted with ethyl acetate (3×10 ml). The organic layer is washed with water (2×10 ml), brine (20 ml), dried over anhydrous sodium sulfate and evaporated to get the crude product, which is purified by column chromatography (silica gel, 25% ethyl acetate/hexane) to yield 2-(ethylsulfonyl)-6-methyl-4-morpholin-4-yl-benzonitrile (0.50 g, 1.70 mmol, 96%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108936B2
Source datasetuspto-grants-2015_08
ORD IDord-a60b109d75a84e7897526f06d9a3cc17
Source noteuspto-grants-2015_08