HuagongsheHuagongshe Chemistry Print Report · For research reference only
(3E)-4-(3-methoxyphenyl)but-3-en-2-one → HCID 23051864, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (3E)-4-(3-methoxyphenyl)but-3-en-2-one | HCID 2560578 | — |
| Reactant | Glyoxylic acid, monohydrate | HCID 15620607 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 23051864 | HCID 23051864 | — |
Reaction Steps
A solution of 14.7 g (83.4 mmol) of (E)-4-(3-methoxyphenyl)but-3-en-2-one and 7.67 g (83.4 mmol) of glyoxylic acid monohydrate in 21.2 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 ether/ethyl acetate yielded (E,E)-6-(3-methoxyphenyl)-4-oxo-2,5-hexadienoic acid of melting point 158°-160°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04927958 |
| Source dataset | uspto-grants-1990_05 |
| ORD ID | ord-3c2143c3e108462e96191b8fe7e706bb |
| Source note | uspto-grants-1990_05 |