HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1-[N-Methyl[2-(4-methoxyphenyloxy)ethyl]carbamoyl]-2-oxopyrrolidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 1-Phenoxycarbonyl-2-oxopyrrolidine | HCID 14441090 | — |
| Reactant | 2-(4-methoxyphenyloxy)ethyl-N-methylamine hydrobromide | HCID 19769860 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 1-[N-Methyl[2-(4-methoxyphenyloxy)ethyl]carbamoyl]-2-oxopyrrolidine | HCID 14441145 | 88.8% |
Reaction Steps
A mixture of 1.87 g (9.13 mmol) of 2-oxo-1-phenoxycarbonylpyrrolidine (II), 2.39 g (9.13 mmol) of 2-(4-methoxyphenyloxy)ethyl-N-methylamine hydrobromide and 2.30 g (22.8 mmol) of triethylamine in 0.5 ml of DMA was heated at 115°-125° C. for 6.5 hr. and ethyl acetate was added to the reaction solution. The mixture was washed with aqueous NaHCO3 and water, and dried, then the solvent was distilled off. The residue was refined by silica gel column chromatography, whereby 2.37 g of an oily compound (Ia-41) was obtained from the eluate with toluene/ethyl acetate (5/1-3/1 v/v). Yield:88.8%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05202345 |
| Source dataset | uspto-grants-1993_04 |
| ORD ID | ord-0e5c8f6fac374436bfe7ca9464f69777 |
| Source note | uspto-grants-1993_04 |