HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Malonate → HCID 10551486, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 4-[2-(5-Methyl-2-phenyloxazol-4-yl)ethoxy]benzaldehyde | HCID 10757106 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 10551486 | HCID 10551486 | 82% |
Reaction Steps
4-[2-(5-Methyl-2-phenyl-4-oxazolyl)ethoxy]benzaldehyde (8.0 g, 26.0 mmol) synthesized according to the method described in WO95/18125, diethyl malonate (4.79 g, 29.9 mmol), acetic acid (1.04 ml) and piperidine (1.03 ml) were mixed. While removing water through Dean-Stark trap, the mixture was refluxed under heating. Three and a half hours later, toluene was evaporated and the obtained residue was recrystallized from ethyl acetate-hexane to give the title compound (9.55 g, yield 82%) as pale-brown white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06204277B1 |
| Source dataset | uspto-grants-2001_03 |
| ORD ID | ord-1677ebc478f44b1aa4bc611119d093b9 |
| Source note | uspto-grants-2001_03 |