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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromooctane | HCID 8140 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Pyridine, 5-octyl-2-[4-(octyloxy)phenyl]- | HCID 3126238 | — |
| Reactant | HCID 178506738 | HCID 178506738 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-octyl-2-(4-octyloxyphenyl)pyridine N-oxide | HCID 54368283 | 65.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05630962 |
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| Source dataset | uspto-grants-1997_05 |
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| ORD ID | ord-4e58e304ac9a499eb2b7ec70627013d7 |
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| Source note | uspto-grants-1997_05 |
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