HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Primaperone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 21559992 | HCID 21559992 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Primaperone | HCID 14641 | 100.8% |
Reaction Steps
A mixture of 2 g of 1-(p-fluorophenyl)-4-piperidino-1-butanol liberated from the hydrochloride, 20 ml of benzene, and 4 g of a fine powder of manganese dioxide was stirred for 8 hours at room temperature. After filtration, the precipitate was washed with 20 ml of benzene. The benzene washings and filtrate were combined and concentrated under reduced pressure to obtain oily γ-piperidino-p-fluorobutyrophenone (2 g in weight; infrared absorption spectrum, ν C=0 1678 cm-1). The said oily product was dissolved in 20 ml of ether, and gaseous hydrogen chloride was introduced therein to saturation. The precipitate formed was recrystallized from ethanol-ether to yield the hydrochloride melting at 180° - 181°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03936468 |
| Source dataset | uspto-grants-1976_02 |
| ORD ID | ord-15cbc24504af4135b7087a758a4202f1 |
| Source note | uspto-grants-1976_02 |