HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 984077Generated: October 29, 2026
4-Piperidinecarboxylic acid → 5-methyl-2-piperidin-4-yl-1,3-benzoxazole
https://huagongshe.com/reaction/984077
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Piperidinecarboxylic acid | HCID 3773 | — |
| Reactant | 2-Amino-4-methylphenol | HCID 7264 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-methyl-2-piperidin-4-yl-1,3-benzoxazole | HCID 22028512 | 83.4% |
Reaction Steps
2-Amino-4-methylphenol (400 mg) and 4-piperidinecarboxylic acid (420 mg) were mixed with polyphosphoric acid (2 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)-5-methylbenzoxazole (586 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-246a26cf328547faad40ab6ff0d49a32 |
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| Source note | uspto-grants-2005_03 |
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