HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 407195Generated: October 31, 2026
1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide → HCID 86670627, compound
https://huagongshe.com/reaction/407195
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide | HCID 339496 | — |
| Reactant | HCID 67153735 | HCID 67153735 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 86670627 | HCID 86670627 | — |
Reaction Steps
To a solution of tert-butyl 4-cyano-4-[4-(hydroxymethyl)pyridine-2-yl]piperidine-1-carboxylate (see Example 23, 0.465 g, 1.46 mmol) in 7 mL of acetonitrile was added 1-hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide (1.23 g, 4.39 mmol). The mixture was heated to 80° C. for 1 h, cooled to rt, and filtered through a glass frit. The filter cake was washed 3× with dichloromethane and the organic filtrate was concentrated in vacuo. The resultant residue was subjected to silica gel chromatography eluting with 0-30% EtOAc in hexanes to provide tert-butyl 4-cyano-4-(4-formylpyridin-2-yl)piperidine-1-carboxylate that gave a proton NMR spectra consistent with theory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08754220B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-44a5770e1a4c4be0b3fd1105feecca58 |
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| Source note | uspto-grants-2014_06 |
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