HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 3-[(2-Methyl-4-oxo-4H-chromen-8-yl)methylene]pentane-2,4-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Acetylacetone | HCID 31261 | — |
| Reactant | 2-Methyl-4-oxo-4H-chromene-8-carbaldehyde | HCID 13374883 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-[(2-Methyl-4-oxo-4H-chromen-8-yl)methylene]pentane-2,4-dione | HCID 59186915 | — |
Reaction Steps
20 g (106 mmol) of 2-methyl-4-oxo-4H-chromene-8-carbaldehyde, 12 ml (116 mmol) of 2,4-pentanedione, 9.1 ml (159 mmol) of acetic acid and 0.21 ml (2.1 mmol) of piperidine in 400 ml of anhydrous dichloromethane are stirred under reflux with a water trap for 24 h. After cooling, the reaction solution is washed successively with saturated sodium bicarbonate solution and saturated sodium chloride solution. The organic phase is dried over magnesium sulfate and concentrated. The residue is recrystallized from isopropanol. 24.3 g (73% of theory) of the title compound are obtained as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08399471B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-7887bc3fb9ca4df381dec5d63020263b |
| Source note | uspto-grants-2013_03 |