HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448299Generated: October 31, 2026
Sodium Hydroxide → 4-Piperidinemethanol, 4-(phenylamino)-1-(2-phenylethyl)-
https://huagongshe.com/reaction/1448299
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 1-phenethyl-4-(phenylamino)piperidine-4-carboxylate | HCID 12298147 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 4-Piperidinemethanol, 4-(phenylamino)-1-(2-phenylethyl)- | HCID 12298204 | — |
Reaction Steps
To a stirred and gently refluxing solution of 43 parts of ethyl 4-(phenylamino)-1-(2-phenylethyl)-4-piperidinecarboxylate in 288 parts of dry benzene is added dropwise a solution of 33.9 parts of sodium dihydro-bis(2-methoxyethoxy)aluminate 70% in 72 parts of dry benzene without heating. Upon completion, stirring is continued for 3 hours at reflux. The reaction mixture is allowed to cool to room temperature overnight and poured onto 1000 parts of ice-water. The resulting emulsion is decomposed by the addition of a concentrated sodium hydroxide solution. The organic layer is separated and filtered over hyflo. The filter-cake is washed thoroughly with benzene. The filtrate is dried, filtered and evaporated. The residue is crystallized from 385 parts of 2,2'-oxybispropane. The crude solid product is filtered off and recrystallized from 2-propanol, yielding 4-(phenylamino)-1-(2-phenylethyl)-4-piperidinemethanol; mp. 96.7° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04179569 |
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| Source dataset | uspto-grants-1979_12 |
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| ORD ID | ord-79f025daf328474c95a4f10938fb0f38 |
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| Source note | uspto-grants-1979_12 |
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