HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Hydrochloric Acid → (E)-1-(4-hydroxyphenyl)-5-(4-morpholinyl)-1-penten-3-one hydrochloride
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Formaldehyde | HCID 712 | — |
| Edukt | Morpholine | HCID 8083 | — |
| Edukt | 3-Buten-2-one, 4-(4-hydroxyphenyl)- | HCID 95648 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | (E)-1-(4-hydroxyphenyl)-5-(4-morpholinyl)-1-penten-3-one hydrochloride | HCID 12842146 | — |
Reaktionsschritte
4.86 g (0.03 mole) of 4-(4-hydroxyphenyl)-3-buten-2-one, 1.2 g (0.04 mole) of paraformaldehyde and 2.6 g (0.03 mole) of morpholine is added to 60 ml of ethanol and 6 ml of concentrated HCl is added thereto. The mixture is heated at reflux temperature for 18 hours and then cooled to room temperature. The resultant mixture is diluted with acetone to a volume of 250 ml and subsequently chilled overnight. The insoluble material is filtered and recrystallized from a mixture of ethyl and methyl alcohols. The crystals are filtered and vacuum dried overnight, yielding (E)-1-(4-hydroxyphenyl)-5-(4-morpholinyl)-1-penten-3-one hydrochloride; m.p. 195°-196° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04400380 |
| Quelldatensatz | uspto-grants-1983_08 |
| ORD ID | ord-bd8d2fed1b9b4ffd89e4cc1aacb584d9 |
| Quellennotiz | uspto-grants-1983_08 |