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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1025411Generated: November 3, 2026

Cyclohexanone → HCID 71238639, compound

https://huagongshe.com/reaction/1025411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanoneHCID 7967—
ReactantMorpholineHCID 8083—
ReactantHCID 71238765HCID 71238765—
SolventTolueneHCID 1140—
ProductHCID 71238639HCID 71238639—

Reaction Conditions

Temperature120 °C

Reaction Steps

To a mixture of 54.0 g of methyl 4-(2-{4-[(cyanoacetyl)amino]phenyl}ethyl)benzoate, 50.0 mL of cyclohexanone, and 300 mL of toluene was added dropwise 15.0 mL of morpholine at room temperature. In a reaction apparatus to which a Dean-Stark type dehydration tube was attached, the reaction mixture was stirred at 120° C. for 3 hours. Subsequently, the reaction mixture was further heated to reflux and stirred for 1 hour. The reaction mixture was cooled to room temperature and then concentrated under reduced pressure. To the residue was further added 200 mL of diisopropyl ether, followed by stirring for 14 hours. The precipitated solid was collected by filtration to obtain 53.2 g of methyl 4-[2-(4-{[cyano(cyclohexylidene)acetyl]amino}phenyl)ethyl]benzoate as a beige solid. ESI+: 403

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729068B2
Source datasetuspto-grants-2014_05
ORD IDord-2d59286a2ef94a06b518aa444597f511
Source noteuspto-grants-2014_05