HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973783Generated: October 31, 2026
Phenethyl bromide → Ethyl 1-phenethyl-4-(phenylamino)piperidine-4-carboxylate
https://huagongshe.com/reaction/1973783
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phenethyl bromide | HCID 7666 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Dimethylacetamide | HCID 31374 | — |
| Reactant | 4-Piperidinecarboxylic acid, 4-(phenylamino)-, ethyl ester | HCID 12298172 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 1-phenethyl-4-(phenylamino)piperidine-4-carboxylate | HCID 12298147 | — |
Reaction Steps
A mixture of 28.7 parts of (2-bromoethyl)benzene, 34.7 parts of ethyl 4-anilinoisonipecotate, 25 parts of N,N-diethylethanamine and 162 parts of N,N-dimethylacetamide is stirred for 2h. 30 at 75°-80° C. The reaction mixture is poured onto 1000 parts of water and the product is extracted three times with 210 parts of 1,1'-oxybisethane. The combined extracts are washed twice with 200 parts of water, dried, filtered and evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and 2% of methanol as eluent. The pure fractions are collected and the eluent is evaporated. The oily residue is crystallized from 2,2'-oxybispropane, yielding ethyl 4-(phenylamino)-1-(2-phenylethyl)-4-piperidinecarboxylate; mp. 65° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03998834 |
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| Source dataset | uspto-grants-1976_12 |
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| ORD ID | ord-e7cbba88ffc94da59c626f577891e6ac |
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| Source note | uspto-grants-1976_12 |
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