HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → 4-Hydroxy-6-methyl-3-(4-nitrophenyl)acryloyl-2-pyrone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | 4-Nitrobenzaldehyde | HCID 541 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Dehydroacetic acid | HCID 122903 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Hydroxy-6-methyl-3-(4-nitrophenyl)acryloyl-2-pyrone | HCID 135406059 | 82% |
Reaction Steps
4-Nitrobenzaldehyde (4.5 g, 29.7 mmol) and then a number of drops of piperidine were added to a benzene (40 ml) solution of dehydroacetic acid (5.00 g, 29.7 mmol) at room temperature, after which refluxing was performed for 6 hours while eliminating water by azeotropy. The majority of the benzene was distilled of directly, and then the distillation taken to dryness under reduced pressure. Following which, when recrystallization was performed from ethanol, 4-hydroxy-6-methyl-3-(4-nitrophenyl)acryloyl-2-pyrone (7.3 g, 82%) was obtained as orange crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06100292 |
| Source dataset | uspto-grants-2000_08 |
| ORD ID | ord-bdada907a2d44d15be6a7dc8e5a6fd8f |
| Source note | uspto-grants-2000_08 |