HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3-(4-Benzyloxyphenyl)-7-methoxymethyloxy-3-methylchroman-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-(4-Hydroxyphenyl)-7-methoxymethyloxy-3-methylchroman-4-one | HCID 22033139 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 3-(4-Benzyloxyphenyl)-7-methoxymethyloxy-3-methylchroman-4-one | HCID 22033223 | 100.5% |
Reaction Steps
To a mixture of 3-(4-hydroxyphenyl)-7-methoxymethyloxy-3-methylchroman-4-one (3.55 g, 11.293 mmol) and potassium carbonate (9.35 g, 67.76 mmol) in acetone (130 ml) was added benzyl bromide (5.795 g, 33.879 mmol) at room temperature and stirred overnight. When the reaction was completed, water was added to the reaction solution which was then extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by column chromatography (n-hexane:ethyl acetate=9:1 to 7:3) to give 4.59 g (yield: quant.) of the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07074819B2 |
| Source dataset | uspto-grants-2006_07 |
| ORD ID | ord-47fba20e611b40fda7efa01f69a68d31 |
| Source note | uspto-grants-2006_07 |