HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1846802Generated: November 1, 2026
HCID 178522112, compound → HCID 178522109, compound
https://huagongshe.com/reaction/1846802
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 178522112 | HCID 178522112 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178522109 | HCID 178522109 | — |
Reaction Steps
trans-3-(benzyloxy)-N-(pyridin-2-yl)cyclobutanecarboxamide (0.394 g, 1.40 mmol) and palladium hydroxide (0.098 g, 0.14 mmol, 20 weight % on carbon) were mixed in ethanol (5 mL). The reaction mixture was placed under a hydrogen atmosphere (balloon) and stirred at 70° C. for 20 h. The reaction mixture was cooled to RT and filtered. The filtrate was concentrated, and the resulting crude product was purified via silica gel chromatography to give trans-3-hydroxy-N-(pyridin-2-yl)cyclobutanecarboxamide as an off white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08952037B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-fad087c2c0884ee58f95d65885fa6bd6 |
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| Source note | uspto-grants-2015_02 |
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