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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxideHCID 339496—
ReactantHCID 67153735HCID 67153735—
SolventAcetonitrileHCID 6342—
ProductHCID 86670627HCID 86670627—

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754220B2
Source datasetuspto-grants-2014_06
ORD IDord-44a5770e1a4c4be0b3fd1105feecca58
Source noteuspto-grants-2014_06