HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → 1-(4-Fluorophenyl)-4-methyl-2-phenyl-penten-3-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 4-Fluorobenzaldehyde | HCID 68023 | — |
| Reactant | Benzyl isopropyl ketone | HCID 76163 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-(4-Fluorophenyl)-4-methyl-2-phenyl-penten-3-one | HCID 54434934 | — |
Reaction Steps
0.9 ml of piperidine is added to 24.8 g (0.2 mol) of 4-fluorobenzaldehyde and 32.4 g (0.2 mol) of benzyl isopropyl ketone in 150 ml of toluene and the mixture is heated to reflux overnight. After cooling to room temperature, the mixture is extracted several times using water and the organic phase is dried over magnesium sulphate and concentrated in vacuo. The residue is subjected to incipient distillation up to a bath temperature of 150° C. at 0.1 mbar in a high vacuum and 43.8 g of crude product are obtained in the distillation residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05401746 |
| Source dataset | uspto-grants-1995_03 |
| ORD ID | ord-2cc95da6d8a14918818e429d848217a4 |
| Source note | uspto-grants-1995_03 |