HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2'-Benzyloxy-6'-hydroxy-4-methylchalcone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Methylbenzaldehyde | HCID 7725 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1-[2-(Benzyloxy)-6-hydroxyphenyl]ethan-1-one | HCID 2775187 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2'-Benzyloxy-6'-hydroxy-4-methylchalcone | HCID 67136326 | — |
Reaction Steps
To a suspension of 2′-benzyloxy-6′-hydroxyacetophenone (0.5 g) in ethanol (10 mL)-water (3 mL) was added potassium hydroxide (1.39 g), and the mixture was stirred at room temperature for 10 minutes. To the reaction mixture was added p-tolualdehyde (0.37 mL), and the mixture was stirred at room temperature for 45 minutes. The reaction mixture was acidified by addition of 2 mol/L hydrochloric acid (12.5 mL), and the precipitated crystals were collected by filtration. The crystals were washed with water and dried under reduced pressure to give the title compound (0.69 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07566699B2 |
| Source dataset | uspto-grants-2009_07 |
| ORD ID | ord-1e42d88d3045493d9652b4c0475eb92d |
| Source note | uspto-grants-2009_07 |