HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 10601391, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 209746-56-5 | HCID 6918439 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 10601391 | HCID 10601391 | 60% |
Reaction Steps
3-(5-Benzo[b]furanyl)-2'-(β-D-glucopyranosyloxy)-6'-hydroxy-4'-methylpropiophenone (2.50 g) is dissolved in acetone (20 ml), and thereto are added potassium carbonate (2.13 g) and allyl bromide (933 mg), and the mixture is refluxed for 6 hours. After cooling, the reaction mixture is poured into ice-water, and the mixture is extracted with ethyl acetate. The organic layer is washed with water, dried, and concentrated under reduced pressure. The resulting residue is purified by silica gel column chromatography (solvent; chloroform/methanol) to give 3-(5-benzo[b]furanyl)-2'-(β-D-glucopyranosyloxy)-6'-allyloxy-4'-methylpropiophenone (1.63 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06048842 |
| Source dataset | uspto-grants-2000_04 |
| ORD ID | ord-22413ed291b94becb6f3eb1d406f315a |
| Source note | uspto-grants-2000_04 |