HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → 7-Methoxy-3-[3-phenyl-1,2,4-oxadiazol-5-yl]coumarin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 2-Hydroxy-4-Methoxybenzaldehyde | HCID 69600 | — |
| Reactant | 3-Phenyl-1,2,4-oxadiazole-5-acetic acid | HCID 7017713 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 7-Methoxy-3-[3-phenyl-1,2,4-oxadiazol-5-yl]coumarin | HCID 21563687 | — |
Reaction Steps
7.6 parts of 2-hydroxy-4-methoxy benzaldehyde and 11.6 parts of the ethyl ester of 3-phenyl-1,2,4-oxadiazole-5-acetic acid (boiling point: 150° C/0.5 mm) are dissolved in 80 parts of toluene. 0.5 part of piperidine is added and the mixture is heated under reflux for 1 hour. The mixture is cooled, the crystallized product is filtered and then washed in ethanol. 13.7 parts of 7-methoxy 3-(3-phenyl 1,2,4-oxadiazol-5-yl) coumarin are obtained which, after crystallization in an ethanol-dioxane mixture, melts at 215° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03994907 |
| Source dataset | uspto-grants-1976_11 |
| ORD ID | ord-17ff0386cf2e4423bc0e5880aaa6b763 |
| Source note | uspto-grants-1976_11 |