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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | 4-(4-Methylphenyl)-3-buten-2-one | HCID 107388 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (E)-1-(4-methylphenyl)-5-(4-morpholinyl)-1-penten-3-one hydrochloride | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04400380 |
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| Source dataset | uspto-grants-1983_08 |
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| ORD ID | ord-5f831d5144b6416ea3bb99e62c3f634f |
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| Source note | uspto-grants-1983_08 |
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