HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 4-Methoxybenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Xanthoxylin | HCID 66654 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 4-Methoxybenzaldehyde | HCID 31244 | 105.1% |
Reaction Steps
To a mixture of 34.7 g of the 2'-hydroxy-4',6'-dimethoxyacetophenone obtained in Production Example 7, 25.3 g of p-anisaldehyde, 150 ml of ethanol and 150 ml of dimethylsulfoxide was added 150 ml of a saturated solution of potassium hydroxide in ethanol at 0° C., and the mixture was stirred at room temperature for 4 hours to effect reaction. After the reaction, the reaction mixture was made acidic by dilute hydrochloric acid to obtain a precipitate. The precipitate was washed with water and recrystallized from a mixed solvent of methanol and ethyl acetate to obtain 43.4 g (yield=78.4%) of 2'-hydroxy-4,4',6'-trimethoxychalcone in the form of a yellow needle.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05106871 |
| Source dataset | uspto-grants-1992_04 |
| ORD ID | ord-35fe829a988b43b4bc56271c95117966 |
| Source note | uspto-grants-1992_04 |