HuagongsheHuagongshe Chemistry Print Report · For research reference only
Homovanillyl alcohol → HCID 69203622, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Homovanillyl alcohol | HCID 16928 | — |
| Reactant | 1-Bromo-4-phenylbutane | HCID 259668 | — |
| Reactant | HCID 178418582 | HCID 178418582 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69203622 | HCID 69203622 | — |
Reaction Steps
To a solution of homovanillyl alcohol (10 g, 59.3 mmol) in dry methanol (140 ml), there is added 12 ml of 1N NaOCH3 in methanol. After addition of a solution of 1-bromo-4-phenylbutane (12.6 g, 59.3 mmol) in THF (10 ml) the reaction mixture is kept at reflux for 3 hours. After cooling the reaction is quenched with saturated aqueous NaHCO3 and extracted with ethyl acetate (2 times, 500 ml each). The organic layer is dried over MgSO4 and the solvent is removed by evaporation. The crude residue is then purified on silica gel using ethyl acetate/n-hexane (1/1) as mobile phase.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07326801B2 |
| Source dataset | uspto-grants-2008_02 |
| ORD ID | ord-51cd0c2816dc44f4b05eafb67ad91eaf |
| Source note | uspto-grants-2008_02 |