HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 19744888, compound → 4-Methoxybenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 19744888 | HCID 19744888 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Methoxybenzaldehyde | HCID 31244 | 101.1% |
Reaction Steps
To a liquid mixture of 11.8 g of the 4',6'-dimethoxy-2'-methoxycarbonylmethoxy-3'-isopentylacetophenone obtained in Production Example 5, 4.8 g of p-anisaldehyde and 50 ml of ethanol was added 150 ml of a saturated solution of potassium hydroxide in ethanol, and the mixture was stirred at room temperature overnight to effect a reaction. After the reaction, the reaction mixture was made acidic by dilute hydrochloric acid, extracted with diethyl ether and filtered, and the solvent was removed from the filtrate by distillation. The obtained residue was recrystallized from a mixed solvent of diethyl ether and n-hexane to obtain 12.7 g (yield=81.9%) of 2'-carboxymethoxy-4,4',6'-trimethoxy-3'-isopentylchalcone in the form of a yellow prism.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05106871 |
| Source dataset | uspto-grants-1992_04 |
| ORD ID | ord-907448f7d4d348f1aab9d346955c8284 |
| Source note | uspto-grants-1992_04 |