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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516958Generated: October 25, 2026

Morpholine → 4-((Morpholin-4-yl)methyl)benzonitrile

https://huagongshe.com/reaction/516958

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantTriethylamineHCID 8471—
Reactant4-(Bromomethyl)benzonitrileHCID 86996—
SolventDichloromethaneHCID 6344—
Product4-((Morpholin-4-yl)methyl)benzonitrileHCID 21686474%

Reaction Steps

To a stirred suspension of 4-(bromomethyl)benzonitrile (4.00 g, 20 mmol) in DCM (50 ml), at room temperature, triethylamine (4.12 g, 41 mmol) and morpholine (2.67 g, 31 mmol) were added. The reaction mixture was stirred overnight at room temperature. The solution was then diluted with DCM (100 ml) and washed with NaHCO3 saturated aqueous solution (50 ml), the organic phase was separated, dried over magnesium sulphate and solvents evaporated under reduced pressure. The product was purified by column chromatography using a 80 g silica gel cartridge and the following gradient: Solvent A: DCM, Solvent B: MeOH, 1 min hold at 100% A followed by 12 min ramp to 2.5% B and then 5 min hold at 2.5% B. The desired fractions were combined and concentrated to dryness under reduced pressure to obtain the desired product as a white solid (3 g, 14.8 mmol, Yield 72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115088B2
Source datasetuspto-grants-2015_08
ORD IDord-81417da16c684df18aea44afe691771e
Source noteuspto-grants-2015_08