HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Methyl-2-butanone → 1-(4-Bromo-phenyl)-4-methyl-pent-1-en-3-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Methyl-2-butanone | HCID 11251 | — |
| Reactant | 4-Bromobenzaldehyde | HCID 70741 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 1-(4-Bromo-phenyl)-4-methyl-pent-1-en-3-one | HCID 374250 | 58.1% |
Reaction Steps
4-Bromo-benzaldehyde (available from Aldrich, 10.0 g, 54.3 mmol) was added to a solution of 3-methyl-butan-2-one (available from Aldrich, 4.7 g, 54.7 mmol) in 10 mL of 10% NaOH(aq) and 20 mL of ethanol. After stirring at room temperature for 3 h, the reaction mixture was diluted with water (50 mL) and extracted with diethyl ether (3×20 mL). The organic layer was then washed with brine (1×5 mL), dried (MgSO4) and concentrated at reduced pressure. Purification by flash chromatography (95:5 hexane/ethyl acetate) yielded the title compound (7.98 g, 58% yield) as a light yellow oil:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07253319B2 |
| Source dataset | uspto-grants-2007_08 |
| ORD ID | ord-001dcec6ce494233aead8ec292cd9027 |
| Source note | uspto-grants-2007_08 |