HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → 4-(3-Methoxy-4-ethoxyphenyl)-3-buten-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Ethoxy-3-methoxybenzaldehyde | HCID 67116 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(3-Methoxy-4-ethoxyphenyl)-3-buten-2-one | HCID 69248120 | 66.5% |
Reaction Steps
10% sodium hydroxide aqueous (40 ml) was added under stirring to a solution of 3-methoxy-4-ethoxybenzaldehyde (9.09 g, 50 mmol) in acetone (25 ml), 95% ethanol (25 ml) and water (200 ml). The reaction mixture was stirred for 24 hr at room temperature, after the reaction completed, the reaction mixture was neutralized with 6N hydrochloric acid to adjust pH=7.0. The precipitated solid was collected by filtrating and washed with water and ethanol successively, dried, and then recrystallized from 95% ethanol to give 7.38 g of a pale yellow solid, mp: 95-97° C., yield: 66.5%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08524744B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-494e067128284a1eb05853ce0472705c |
| Source note | uspto-grants-2013_09 |