HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 14257849, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (3-Bromopropyl)benzene | HCID 12503 | — |
| Reactant | Phenyl(piperidin-4-yl)methanone | HCID 226102 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Toluene ethylacetate | HCID 21584019 | — |
| Solvent | Ethylacetate methanol | HCID 21584119 | — |
| Product | HCID 14257849 | HCID 14257849 | — |
Reaction Steps
A solution of phenyl (4-piperidinyl)methanone (18.1 g, 0.096 mol) was dissolved in toluene (200 ml) containing 1-bromo-3-phenylpropane (21.9 g, 0.11 mol, 16.7 ml), K2CO3 (30.4 g, 0.22 mol) and KI (0.2 g ) and was refluxed for 64 h. The reaction mixture was filtered and concentrated to give a light yellow oil. This material was dissolved in toluene/EtOAc (1:1) and treated with HCl (0.096 mol) dissolved in CH3OH/EtOAc (2:5, 35 ml) to give a precipitate which was filtered off and recrystallized twice from EtOH/Et2O (150 ml) to give phenyl[1-(3-phenylpropyl)-4-piperidinyl)-methanone hydrochloride, mp 199°-200° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04912117 |
| Source dataset | uspto-grants-1990_03 |
| ORD ID | ord-c19afd1e50434f75b3b502e7adfdc0a8 |
| Source note | uspto-grants-1990_03 |