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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 435111Generated: October 25, 2026

Hydrochloric Acid → (E)-1-(4-methylphenyl)-5-(4-morpholinyl)-1-penten-3-one hydrochloride

https://huagongshe.com/reaction/435111

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFormaldehydeHCID 712—
ReactantMorpholineHCID 8083—
Reactant4-(4-Methylphenyl)-3-buten-2-oneHCID 107388—
SolventAcetoneHCID 180—
SolventEthanolHCID 702—
Product(E)-1-(4-methylphenyl)-5-(4-morpholinyl)-1-penten-3-one hydrochlorideHCID 12842152—

Reaction Steps

8 g (0.05 mole) of 4-(4-methylphenyl)-3-buten-2-one (prepared analogously to the intermediates for the foregoing examples), 2 g (a 30% excess) of paraformaldehyde and 4.35 g (0.05 mole) of morpholine are dissolved in a mixture of ethanol (60 ml) and concentrated HCl (6 ml). The mixture is heated at reflux temperature for 18 hours. The mixture is then cooled to room temperature and diluted with acetone to a volume of 250 ml. The solution is chilled overnight. It is then concentrated to a volume of about 25 ml. The residue is triturated with ethyl alcohol. The insoluble material is filtered and recrystallized from ethyl alcohol/methyl alcohol. The resultant crystals are filtered and vacuum dried overnight, yielding 3.3 g of (E)-1-(4-methylphenyl)-5-(4-morpholinyl)-1-penten-3-one hydrochloride; m.p. 188°-190° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04400380
Source datasetuspto-grants-1983_08
ORD IDord-5f831d5144b6416ea3bb99e62c3f634f
Source noteuspto-grants-1983_08