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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1645544Generated: October 30, 2026

Sodium hydride → 4-(5,9-Dioxaspiro[3.5]non-7-yloxy)-2,3-dimethylpyridine 1-oxide

https://huagongshe.com/reaction/1645544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant4-Chloro-2,3-dimethyl-1-oxidopyridin-1-iumHCID 9877446—
Reactant5,9-Dioxaspiro[3.5]nonan-7-olHCID 57823108—
SolventDimethylformamideHCID 6228—
Product4-(5,9-Dioxaspiro[3.5]non-7-yloxy)-2,3-dimethylpyridine 1-oxideHCID 5782310564.4%

Reaction Steps

To a dimethyl formamide (30 ml) solution of the 5,9-dioxaspiro[3.5]nonan-7-ol (1.68 g, 11.7 mmol) obtained in the step (9e), sodium hydride, in oil (587 mg, 13.5 mmol as the content was regarded as 55%) was added at room temperature. The mixture was stirred at room temperature for 50 minutes. After 4-chloro-2,3-dimethylpyridine 1-oxide (1.84 g, 11.7 mmol) was added thereto, the mixture was stirred at 80° C. for 2 hours. The reaction mixture was concentrated and dimethylsulfoxide (30 ml) was added thereto and stirred at 80° C. After 12 hours, sodium hydride, in oil (587 mg, 13.5 mmol as the content was regarded as 55%) was added to the reaction mixture and stirred at 80° C. After one hour, the reaction mixture was concentrated and the residue was purified by silica gel column chromatography (NH silica gel, elution solvent: ethyl acetate, ethyl acetate/methanol=9/1) to obtain the title compound (2.00 g, yield: 64.4%) as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124780B2
Source datasetuspto-grants-2012_02
ORD IDord-435ba6b6616043bbb3149f0e0be286fd
Source noteuspto-grants-2012_02