HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetophenone → 2-Phenyl-4-penten-2-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetophenone | HCID 7410 | — |
| Reactant | HCID 178455850 | HCID 178455850 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Phenyl-4-penten-2-ol | HCID 143761 | 99.1% |
Reaction Steps
To a solution of acetophenone (30 g, 0.25 mol) in dry THF (250 mL) at −78° C. was added dropwise 1M allylmagnesium bromide (1.25 L, 1.25 mol). After addition was complete, the mixture was allowed to stir at rt for 3 h. The reaction was quenched with satd aq NH4Cl solution (30 mL). The mixture was extracted with EtOAc (200 mL). The organic layer was washed with brine (30 mL), dried over anhydrous Na2SO4 and concentrated to give 2-phenylpent-4-en-2-ol (40.2 g), which was used for the next step without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08487094B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-19e7be6426b942bda5c4d5b18941ffbb |
| Source note | uspto-grants-2013_07 |