HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Cinnamoylbenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 3,4,5-Trimethoxybenzaldehyde | HCID 6858 | — |
| Reactant | 3',4',5'-Trimethoxyacetophenone | HCID 14345 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Potassium Carbonate | HCID 11430 | — |
| Product | Cinnamoylbenzene | HCID 7189 | — |
Reaction Steps
To a stirred solution of 3,4,5-trimethoxybenzaldehyde (190 mg, formula 5) in 10% methanolic potassium carbonate (15 mL), 3,4,5-trimethoxyacetophenone (200 mg) was added. It was stirred for 3 hours. On completion, the reaction mixture was diluted with water, acidified with dil. HCl and extracted with ethyl acetate. The organic layer was washed with water, dried over anhydrous sodium sulphate and evaporated to get a residue. The residue was purified through silica gel column to get chalcone of formula 6 (240 mg)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08633242B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-0c93a4b94d1a437bbadeef6314b011a7 |
| Source note | uspto-grants-2014_01 |