Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Piperidine, 1-(2-chloroethyl)-, hydrochloride | HCID 74826 | — |
| Reactant | 4-Benzhydrylpiperidine | HCID 88278 | — |
| Reactant | 1-(2-Piperidinoethyl)-4-(diphenylmethyl)piperidine | HCID 20315689 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20315688 | HCID 20315688 | — |
Reaction Steps
Following Scheme I, 18.1 parts of 4-diphenylmethylpiperidine (U.S. Pat. No. 3,806,526) 13.6 parts of 2-chloroethylpiperidine hydrochloride and 16 parts of sodium carbonate are placed in 250 parts of aqueous 95% ethanol and heated at reflux for 5 hours with stirring. The ethanol is removed to provide an oil which is 1-(2-piperidinoethyl)-4-(diphenylmethyl)piperidine. This oil is dissolved in anhydrous ethanol and 2 equivalents of hydrochloric acid gas are added to provide 1-(2-piperidinoethyl)-4-(diphenylmethyl)piperidine dihydrochloride, melting at 330° C. The anhydrous ethanol solution of 1-(2-piperidinoethyl)-4-(diphenylmethyl)piperidine is reacted with 1.5 equivalents of oxalic acid to provide the oxalic acid salt. In a similar manner other previously mentioned pharmaceutically acceptable salts are formed.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04105849 |
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| Source dataset | uspto-grants-1978_08 |
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| ORD ID | ord-dd096a6207734e7b9b1dcffdf792d7c1 |
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| Source note | uspto-grants-1978_08 |
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