HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732343Generated: November 1, 2026
HCID 20306038, compound → HCID 20306009, compound
https://huagongshe.com/reaction/1732343
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 20306038 | HCID 20306038 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 20306009 | HCID 20306009 | 9.7% |
Reaction Steps
4-[2-(N-acetyl-4-piperidyloxy)ethoxy]benzamide (4.3 g.) in ethanol (60 ml.), water (30 ml.) and 2 N hydrochloric acid (10 ml.) was heated under reflux for 24 hours then the solvent evaporated in vacuo. The residue was taken up in water and extracted three times with chloroform, the aqueous phase was adjusted to pH 12 with sodium carbonate solution and extracted three times with chloroform. The combined chloroform extracts were discarded, the aqueous phase was saturated with sodium chloride and extracted with chloroform, the chloroform layer dried (Na2SO4), and the solvent evaporated in vacuo to give 4-[2-(4-piperidyloxy)ethoxy]benzamide (0.36 g.). The aqueous phase was concentrated in vacuo and the residual solid extracted with refluxing ethyl acetate (200 ml.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04237138 |
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| Source dataset | uspto-grants-1980_12 |
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| ORD ID | ord-8ea00480d80b453381454ecc413ea5d3 |
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| Source note | uspto-grants-1980_12 |
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