HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → HCID 21563690, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 2-Hydroxy-4-Methoxybenzaldehyde | HCID 69600 | — |
| Reactant | HCID 21494400 | HCID 21494400 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21563690 | HCID 21563690 | — |
Reaction Steps
4.5 parts of 2-hydroxy-4-methoxy benzaldehyde and 7.38 parts of the ethyl ester of 3-p-tolyl-1,2,4-oxadiazol-5-acetic acid (melting point: 56° C) are dissolved in 80 parts of ethanol. 0.3 part of piperidine is added and the mixture is heated for 1 hour under reflux. After cooling, the crystalline precipitate obtained is filtered and washed in ethanol. Thus 8.5 parts of 7-methoxy-3-(3-p-tolyl-1,2,4-oxadiazol-5-yl) coumarin are obtained which melts at 227° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03994907 |
| Source dataset | uspto-grants-1976_11 |
| ORD ID | ord-f21d340476be430997e18daa1c8b9974 |
| Source note | uspto-grants-1976_11 |