HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 20474272, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Ethyl 4-nitrophenylacetate | HCID 79517 | — |
| Reactant | HCID 12412922 | HCID 12412922 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20474272 | HCID 20474272 | 55% |
Reaction Steps
50.6 g (200 mmols) of the Na salt of 2-hydroxy-4-(4-ethyl-5-methyl-2H-1,2,3-triazol-2-yl)-benzaldehyde, 41.8 g (200 mmols) of ethyl 4-nitrophenylacetate and 2 ml of piperidine are refluxed in 250 ml of ethanol for 4 hours. After the mixture has been cooled, it is neutralised with glacial acetic acid, and the residue is washed with ethanol and water, and dried: 46.3 g (61.5%). Recrystallisation from toluene yields 41.4 g (55%) of 3-(4-nitrophenyl)-7-(4-ethyl-5-methyl-2H-1,2,3-triazol-2-yl)-coumarin in the form of a pale yellow crystalline powder of melting point 278°-279° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04426530 |
| Source dataset | uspto-grants-1984_01 |
| ORD ID | ord-ba219a2abac0453aaa637d8ed74a58d1 |
| Source note | uspto-grants-1984_01 |