Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1025413Generated: October 28, 2026

Cyclohexanone → HCID 71238801, compound

https://huagongshe.com/reaction/1025413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanoneHCID 7967—
ReactantMorpholineHCID 8083—
ReactantHCID 71238730HCID 71238730—
SolventTolueneHCID 1140—
ProductHCID 71238801HCID 71238801—

Reaction Steps

To a mixture of 19.3 g of methyl 4-(3-{4-[(cyanoacetyl)amino]phenyl}propyl)benzoate, 18 mL of cyclohexanone, and 100 mL of toluene was added dropwise 5.0 mL of morpholine at room temperature. In a reaction device in which a Dean-Stark type dehydration tube was installed, the reaction mixture was stirred for 8 hours under heating and refluxing. The reaction mixture was cooled to room temperature and then concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (n-hexane-chloroform and ethyl acetate-chloroform) to obtain methyl 4-[3-(4-{[cyano(cyclohexylidene)acetyl]amino}phenyl)propyl]benzoate in the form of a reddish brown amorphous substance as a crude product. ESI+: 417

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729068B2
Source datasetuspto-grants-2014_05
ORD IDord-a0e3e7236ff449e58ea8a972079e68b8
Source noteuspto-grants-2014_05