HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485088Generated: November 1, 2026
1-(4-Biphenyl)-1-propanol → p-Phenylpropiophenone
https://huagongshe.com/reaction/1485088
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-(4-Biphenyl)-1-propanol | HCID 13130482 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | p-Phenylpropiophenone | HCID 95230 | 73.2% |
Reaction Steps
To a solution in diethyl ether (30.0 mL) of the compound (1.27 g) obtained in step (1) above, manganese(IV) oxide (9.57 g) was added and the mixture was stirred at room temperature for 45 hours. After removing the insoluble matter by filtration, the filtrate was concentrated under reduced pressure. To a solution of the resulting residue in acetone (60.0 mL), a Jones' reagent {see Org. Synth., Coll. Vol. VI, 542 (1988)}(1.20 mL) was added until the color of the Jones' reagent was yet to disappear. The reaction mixture was concentrated under reduced pressure and ethyl acetate and water were added to the residue. Extraction with ethyl acetate was conducted three times and the combined organic layers were washed with saturated brine. After passage through a phase separator, the washed organic layers were concentrated under reduced pressure. The resulting residue was recrystallized with n-hexane to give the titled compound as a colorless solid (921 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09422240B2 |
|---|
| Source dataset | uspto-grants-2016_08 |
|---|
| ORD ID | ord-fa03332dda2e4c59880616176888c9fe |
|---|
| Source note | uspto-grants-2016_08 |
|---|