HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448285Generated: October 31, 2026
2-Bromopropane → 1-Methylethyl 4-(phenylamino)-1-(2-phenylethyl)-4-piperidinecarboxylate
https://huagongshe.com/reaction/1448285
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Bromopropane | HCID 6358 | — |
| Reactant | Hexamethylphosphoramide | HCID 12679 | — |
| Reactant | 4-Piperidinecarboxylic acid, 4-(phenylamino)-1-(2-phenylethyl)- | HCID 616233 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Methylethyl 4-(phenylamino)-1-(2-phenylethyl)-4-piperidinecarboxylate | HCID 12298149 | — |
Reaction Steps
A mixture of 10.4 parts of 4-(phenylamino)-1-(2-phenylethyl)-4-piperidinecarboxylic acid, sodium salt and 75 parts of hexamethylphosphoric triamide is stirred and heated at 110° C. for a while. It is cooled to 20° C. and 3.7 parts of 2-bromopropane are added dropwise. After stirring for 4 hours, another 0.37 parts of 2-bromopropane is added dropwise. Upon completion, stirring is continued over week-end at room temperature. The reaction mixture is poured onto 150 parts of water and the product is extracted with methylbenzene. The extract is washed with water, dried, filtered and evaporated. The oily residue is dissolved in 1,1'-oxybisethane. The solution is stirred with activated charcoal. The latter is filtered off and the filtrate is evaporated. The oily residue is crystallized from hexane. The product is filtered off and recrystallized from hexane, yielding 1-methylethyl 4-(phenylamino)-1-(2-phenylethyl)-4-piperidinecarboxylate; mp. 78.5° 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-c9760db79b1b49c7bf6526843a6d0e75 |
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| Source note | uspto-grants-1979_12 |
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