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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 902009Generated: October 29, 2026

4-Benzylpyridine → HCID 86600924, compound

https://huagongshe.com/reaction/902009

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BenzylpyridineHCID 16458—
ReactantO-(2,4,6-Trimethylbenzenesulfonyl)hydroxylamineHCID 11830845—
SolventDichloromethaneHCID 6344—
ProductHCID 86600924HCID 8660092473.9%

Reaction Steps

A solution of 4-benzyl pyridine (0.6 g, 3.5 mmol) in methylene chloride (5 ml) is cooled with ice bath. Freshly prepared O-(2,4,6-trimethyl-benzenesulfonyl)hydroxylamine (0.92 g, 4.2 mmol) in methylene chloride (5 ml) is added dropwise with stirring. The ice bath is removed and the mixture stirred for 1 hour, then concentrated in vacuo. The residue is dissolved in methylene chloride and precipitated with hexanes. The hexane layer is decanted. Concentration provides 1.0 g (62%) of the title compound as a viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07365066B2
Source datasetuspto-grants-2008_04
ORD IDord-2b021d9745f045649e721c4701e7cc4c
Source noteuspto-grants-2008_04