HuagongsheHuagongshe Chemistry Print Report · For research reference only
2',4',6'-Trihydroxyacetophenone → 1-[2,4,6-Trihydroxy-3,5-di(3-methyl-2-buten-1-yl)phenyl]ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2',4',6'-Trihydroxyacetophenone | HCID 68073 | — |
| Reactant | 4-Bromo-2-methylbut-1-ene | HCID 549585 | — |
| Solvent | Potassium Hydroxide | HCID 14797 | — |
| Product | 1-[2,4,6-Trihydroxy-3,5-di(3-methyl-2-buten-1-yl)phenyl]ethanone | HCID 10979627 | 38.7% |
Reaction Steps
1-(2,4,6-trihydroxyphenyl]ethanone (2.0 mg, 11.9 mmol) was dissolved in a 5% potassium hydroxide aqueous solution (20 mL). After the mixture was cooled below 0° C., isopentenyl bromide (3.6 g, 24 mmol) was slowly added dropwise within 30 min. The reaction mixture was stirred at room temperature for 2 hours, then poured into an ice water and acidified to pH 2. The reaction mixture was extracted with ethyl acetate. The extract was collected and dried over anhydrous sodium sulfate. After removal of the solvent, the residue was purified by silica gel column chromatography (dichloromethane as eluent) to give the desired compound (0.7 g, yield 20%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09090583B2 |
| Source dataset | uspto-grants-2015_07 |
| ORD ID | ord-3cb7b15b61034ec69b25282892b2f98a |
| Source note | uspto-grants-2015_07 |