HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 868452Generated: October 31, 2026
(4-Nitrophenyl)acetic acid → HCID 54082859, compound
https://huagongshe.com/reaction/868452
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (4-Nitrophenyl)acetic acid | HCID 4661 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 53781093 | HCID 53781093 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 54082859 | HCID 54082859 | — |
Reaction Steps
A one liter three necked flask fitted with a dropping funnel, mechanical stirrer, and condenser is charged with 34.35 g of 4-nitrophenylacetic acid. Piperidine (16.2 g) is added dropwise over a period of 30 minutes. At the end of the addition period, 44.46 g of 4-[N-(2-hydroxyethyl)piperazinyl]benzaldehyde is added. The mixture is heated at 100° C. for three hours, and at 130° C. for three hours. After cooling, the resultant semi-solid mass is ground up in ethanol in a blender, then filtered, washed with water, and vacuum dried. The crude solid is recrystallized from chlorobenzene: m.p. 221°-224° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04779961 |
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| Source dataset | uspto-grants-1988_10 |
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| ORD ID | ord-e803607ca97543d1a4aa2e0c72f0d7a3 |
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| Source note | uspto-grants-1988_10 |
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