HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (E)-4-(3-(4-hydroxy-3-methylphenyl)-3-oxoprop-1-enyl)benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Formylbenzoic acid | HCID 12088 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4'-Hydroxy-3'-methylacetophenone | HCID 70135 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | (E)-4-(3-(4-hydroxy-3-methylphenyl)-3-oxoprop-1-enyl)benzoic acid | HCID 57831176 | 88.6% |
Reaction Steps
Commercially available 4-formylbenzoic acid (15.0 g, 0.1 mol) and commercially available 4′-hydroxy-3′-methylacetophenone (15.0 g, 0.1 mol) were dissolved in 150 mL of methanol and 50 mL of water. The solution was cooled with an ice-water bath, to which was added potassium hydroxide (28.0 g, 0.5 mol). The reaction mixture was stirred overnight. The resulted mixture was poured on to 600 mL of ice-water, acidified to pH=4-5 with 1 M HCl, filtered, washed with water (200 mL), and dried in the air. 25 g (87%) of a yellowish solid was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08242129B2 |
| Source dataset | uspto-grants-2012_08 |
| ORD ID | ord-e92557d2fc8148fe846576ecf620b9cd |
| Source note | uspto-grants-2012_08 |