HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706739Generated: October 29, 2026
Potassium Hydroxide → HCID 23339051, compound
https://huagongshe.com/reaction/1706739
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 23339044 | HCID 23339044 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 23339051 | HCID 23339051 | — |
Reaction Steps
To a stirred and warm (40° C.) solution of 12 parts of potassium hydroxide in 200 parts of 2-propanol are added at once 21 parts of ethyl 4-{N-(4-chlorophenyl)-N-[(3-methoxyphenyl)acetyl]amino}-1-piperidinecarboxylate and the whole is stirred and refluxed for 17 hours. The reaction mixture is cooled, filtered and evaporated. The semi-solid residue is acidified with a diluted hydrochloric acid solution, washed with 1,1'-oxybisethane and the aqueous acid phase is alkalized with sodium hydroxide solution. The free base is extracted with trichloromethane. The extract is dried and evaporated. The residue is crystallized from a mixture of 1,1'-oxybisethane and hexane, yielding 7.8 parts of N-(4-chlorophenyl)-3-methoxy-N-(4-piperidinyl)benzeneacetamide; mp. 85.7° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04208418 |
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| Source dataset | uspto-grants-1980_06 |
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| ORD ID | ord-2018c904605442dda987a4cb2bbfd2d9 |
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| Source note | uspto-grants-1980_06 |
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