HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → HCID 70594250, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Phenethyl bromide | HCID 7666 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 20343975 | HCID 20343975 | — |
| Reactant | HCID 20343976 | HCID 20343976 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 70594250 | HCID 70594250 | — |
Reaction Steps
A mixture of 0.67 g of 4-ethoxycarbonyl-4-(2-phenylthiophenyl)piperidine, free base of Example 17, 0.48 g of 2-bromoethylbenzene, 0.65 g of sodium bicarbonate and 0.65 g of potassium iodide in 15 ml of dimethylformamide is stirred at 60°-70° C. for 16 hours. Thereafter, the mixture is diluted with ether and the diluted mixture is filtered. The filtrate is concentrated in vacuo. The residue is purified by column chromatography (alumina column, ether eluant) to provide a purified product which, in ether, is converted to its hydrobromic acid salt. The salt is recrystallized from an acetone-ether mixture to provide 4-ethoxycarbonyl-1-phenylethyl-4-(2-phenylthiophenyl)piperidine hydrobromide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04198419 |
| Source dataset | uspto-grants-1980_04 |
| ORD ID | ord-15c26c9bfc9f4dac9f4a141312410256 |
| Source note | uspto-grants-1980_04 |