HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 984076Generated: October 28, 2026
4-Piperidinecarboxylic acid → 2-(Piperidin-4-yl)-1,3-benzoxazole
https://huagongshe.com/reaction/984076
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Piperidinecarboxylic acid | HCID 3773 | — |
| Reactant | 2-Aminophenol | HCID 5801 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(Piperidin-4-yl)-1,3-benzoxazole | HCID 770461 | 84.3% |
Reaction Steps
2-Aminophenol (200 mg) and 4-piperidinecarboxylic acid (236 mg) were mixed with polyphosphoric acid (1 g) and stirred with heating at 180° C. for 2 hours. After cooling to room temperature, the reaction was stopped by adding water. The filtrate was adjusted to pH 12 with 50% potassium hydroxide aqueous solution and then extracted with methylene chloride. The organic layer was washed with saturated brine and dried with magnesium sulfate, and then the solvent was evaporated under a reduced pressure to obtain the title compound 2-(4-piperidyl)benzoxazole (311.5 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06867226B2 |
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| Source dataset | uspto-grants-2005_03 |
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| ORD ID | ord-5a673342a17d4a358448b3a8235e5104 |
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| Source note | uspto-grants-2005_03 |
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