HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperonylidene acetone → HCID 23051852, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperonylidene acetone | HCID 6040503 | — |
| Reactant | Glyoxylic acid, monohydrate | HCID 15620607 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 23051852 | HCID 23051852 | — |
Reaction Steps
A solution of 15 g (78.8 mmol) of (E)-4-[3,4-(methylenedioxy)phenyl]but-3-en-2-one and 7.2 g (78.8 mmol) of glyoxylic acid monohydrate in 20 ml of acetic acid was heated at reflux for 20 hours. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic phase was extracted twice with 3N sodium hydroxide solution. The combined aqueous phases were treated with 3N hydrochloric acid to produce a strongly acidic reaction and extracted twice with ethyl acetate. The combined organic phases were dried over magnesium sulphate and concentrated. Crystallization of the residue from ethyl acetate/ether yielded (E,E)-6-[3,4-(methylenedioxy)phenyl]-4-oxo-2,5-hexadienoic acid of melting point 170°-173°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04927958 |
| Source dataset | uspto-grants-1990_05 |
| ORD ID | ord-cd870529b9d54c86a3c4e11a54da9a60 |
| Source note | uspto-grants-1990_05 |