HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 54104549, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 19978914 | HCID 19978914 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Product | HCID 54104549 | HCID 54104549 | 203.4% |
Reaction Steps
An ethanolic (50 mL) solution of the above N-aryl-2-ethylamino-2-phenylacetamide prepared in Example II (6.8 grams, 0.02 mol) and paraformaldehyde (0.65 grams, 0.02 mol) and potassium carbonate (1.5 grams, 0.01 mol) was heated under reflux for 2 hours. The reaction was followed by thin layer chromatography (3:1 hexane-ethyl acetate). The mixture was concentrated in a rotary evaporator. The product was extracted into ethyl acetate and washed with water and isolated to give the desired 1-ethyl-5-phenyl-3-(3-trifluoromethylphenyl) imidazolidine-4-one (6.8 grams, 97% yield) whose structure was confirmed by nuclear magnetic resonance, infra-red spectroscopy, and mass spectroscopy analysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05076832 |
| Source dataset | uspto-grants-1991_12 |
| ORD ID | ord-0de9eff09ce04e34a5e3dc06882a5c0c |
| Source note | uspto-grants-1991_12 |