HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 1-{1-[2-Hydroxy-3-(2-methoxyphenoxy)-propyl]-4-piperidyl}-3-(4-methoxy-phenyl)-imidazolidin-2-one-hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | ((o-Methoxyphenoxy)methyl)oxirane | HCID 98357 | — |
| Reactant | 1-(4-Methoxyphenyl)3-(4-piperidyl)-2-imidazolidinone | HCID 23347336 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 1-{1-[2-Hydroxy-3-(2-methoxyphenoxy)-propyl]-4-piperidyl}-3-(4-methoxy-phenyl)-imidazolidin-2-one-hydrochloride | HCID 23347350 | — |
Reaction Steps
A mixture of 17.9 g of 1-[4-methoxy-phenyl)-3-(4-piperidyl)-2-imidazolidinone and 11.7 g of 1-(2-methoxyphenyloxy)-2,3-epoxypropane in 200 ml of isopropyl alcohol is refluxed for 6 hours. The mixture is thereafter acidified with 5N methanolic hydrochloric acid and concentrated under reduced pressure. The residue is freed from moisture still adhering to it by treatment with toluene. Recrystallisation of the residue from methanol with the addition of activated charcoal yields the 1-{1-[2-hydroxy-3-(2-methoxyphenoxy)-propyl]-4-piperidyl}-3-(4-methoxy-phenyl)-imidazolidin-2-one-hydrochloride as a white crystalline substance with a melting point of 214°-215° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04144344 |
| Source dataset | uspto-grants-1979_03 |
| ORD ID | ord-b2da3d3a4b7b4524a8e73d1382bc0e3e |
| Source note | uspto-grants-1979_03 |