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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1780542Generated: October 26, 2026

1-Bromooctane → 5-octyl-2-(4-octyloxyphenyl)pyridine N-oxide

https://huagongshe.com/reaction/1780542

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromooctaneHCID 8140—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantPyridine, 5-octyl-2-[4-(octyloxy)phenyl]-HCID 3126238—
ReactantHCID 178506738HCID 178506738—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
Product5-octyl-2-(4-octyloxyphenyl)pyridine N-oxideHCID 5436828365.2%

Reaction Steps

A solution of 3.03 g (12.3 mmol) of 3-chloroperbenzoic acid in 30 ml of methylene chloride is added dropwise at a temperature of 0° to 5° C. to 3.23 g (8.2 mmol) of 5-octyl-2-(4-octyloxyphenyl)pyridine (prepared, for example, analogously to C. S. Giam, J. Staut, J. Chem. Soc., Chem. Commun. 478 (1970) from pyridine, 4-octyloxyphenyllithium and 1-bromooctane) in 30 ml of methylene chloride. After a reaction time of 3 hours at room temperature, the mixture is washed once with 5% sodium carbonate and twice with sodium chloride solution, the organic phase is dried over sodium sulfate, filtered off, and the solvent is removed by distillation. Purification of the residue by chromatography (silica gel, 8:2 methylene chloride/ethyl acetate) gives 2.20 g of 5-octyl-2-(4-octyloxyphenyl)pyridine N-oxide. ##STR13##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05630962
Source datasetuspto-grants-1997_05
ORD IDord-4e58e304ac9a499eb2b7ec70627013d7
Source noteuspto-grants-1997_05