HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Chloride → 1-(Phenylmethyl)-4-piperidinecarboxylic acid ethyl ester hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Ethyl 4-piperidinecarboxylate | HCID 70770 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(Phenylmethyl)-4-piperidinecarboxylic acid ethyl ester hydrochloride | HCID 70092284 | — |
Reaction Steps
A mixture of 100 g (0.637 mole) of ethyl isonipecotate, 80.64 g (0.64 mole) of benzyl chloride and 67.84 g (0.64 mole) of sodium carbonate in 1 liter of absolute ethanol was refluxed for 8 hours and then was stirred at room temperature for 10 hours. The solvent was removed in vacuo, and the residue was partitioned between methylene chloride and dilute sodium hydroxide. The methylene chloride phase was dried over magnesium sulfate, and the solvent was removed in vacuo to give the free base of the title compound as a liquid. The free base was converted to the hydrochloride salt, and the salt was recrystallized from ethanol-ether to give 89.33 g (49.7%) of white, crystalline solid, m.p. 154°-155° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04886794 |
| Source dataset | uspto-grants-1989_12 |
| ORD ID | ord-1e7565d87f794d9bbb227050681b4aa6 |
| Source note | uspto-grants-1989_12 |