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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282477Generated: November 1, 2026

Morpholine → 4-Morpholinobenzonitrile

https://huagongshe.com/reaction/1282477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
Reactant4-ChlorobenzonitrileHCID 12163—
ReactantAmmonium ChlorideHCID 25517—
ReactantCy-vBRIDPHCID 12010824—
ReactantSodium t-butoxideHCID 23676156—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
Product4-MorpholinobenzonitrileHCID 39480881%

Reaction Conditions

Temperature100 °C

Reaction Steps

Into a reactor were introduced 0.275 g (2.00 mmol) of 4-chlorobenzonitrile and 4 mL of toluene under a nitrogen atmosphere. The nitrile was dissolved in the solvent. To this solution were added 0.192 g (2.2 mmol) of morpholine, 0.231 g (2.4 mmol) of sodium t-butoxide, 4.5 mg (1 mol % based on the amine) of palladium acetate, and 15.6 mg (2 mmol % based on the amine) of the 1,1-diphenyl-2(dicyclohexylphosphino)propene obtained in Example 2. The resultant reaction mixture was stirred at 100° C. for 14 hours and then cooled. Saturated aqueous ammonium chloride solution was added thereto, and this mixture was extracted with toluene. The extract was dried with anhydrous magnesium sulfate. Thereafter, the solvent was removed under reduced pressure. The concentrate was purified by column chromatography to obtain 0.304 g (81%) of N-(4-cyanophenyl)morpholine as light-yellow crystals. The results obtained are shown in Table 20.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06455720B1
Source datasetuspto-grants-2002_09
ORD IDord-16f433635de14a6bbf2f73c864ef482c
Source noteuspto-grants-2002_09