Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1245834Generated: October 31, 2026

Acetonitrile → 3-[4-(Morpholin-4-ylmethyl)phenyl]-3-oxopropanenitrile

https://huagongshe.com/reaction/1245834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 4-(morpholin-4-ylmethyl)benzoateHCID 10466592—
SolventTetrahydrofuranHCID 8028—
Product3-[4-(Morpholin-4-ylmethyl)phenyl]-3-oxopropanenitrileHCID 21914496—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of acetonitrile (1.35 ml) in tetrahydrofuran (80 ml), cooled to 5° C., was added sodium hydride (0.94 g, 60% dispersion in oil). The mixture was stirred for 30 minutes before the addition of a solution of methyl 4-(morpholin-4-ylmethyl)benzoate (5.53 g) in tetrahydrofuran (20 ml). The resulting mixture was heated to 70° C. for 5 h. The mixture was cooled, quenched with saturated ammonium chloride (20 ml) and extracted with ethyl acetate. The organic extracts were dried (MgSO4) and evaporated to give a gum which was purified by column chromatography eluting with a 20–100% ethyl acetate/iso-hexane gradient to give 3-[4-(morpholin-4-ylmethyl)phenyl]-3-oxopropanenitrile (0.97 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07125896B2
Source datasetuspto-grants-2006_10
ORD IDord-d0c90b18e23e4ef38a3949ee140d8c99
Source noteuspto-grants-2006_10