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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1645558Generated: October 30, 2026

Sodium hydride → 4-((2,2-Dimethyl-1,3-dioxan-5-yl)methoxy)-2,3-dimethylpyridine 1-oxide

https://huagongshe.com/reaction/1645558

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant(2,2-Dimethyl-1,3-dioxan-5-yl)methanolHCID 3584869—
Reactant4-Chloro-2,3-dimethyl-1-oxidopyridin-1-iumHCID 9877446—
SolventDimethyl SulfoxideHCID 679—
Product4-((2,2-Dimethyl-1,3-dioxan-5-yl)methoxy)-2,3-dimethylpyridine 1-oxideHCID 5979242474.8%

Reaction Steps

To a dimethyl sulfoxide (30 ml) solution of the (2,2-dimethyl-1,3-dioxan-5-yl)methanol (3.27 g, 22.4 mmol) separately obtained in the same manner as in the step (11a) in example 11, sodium hydride, in oil (837 mg, 20.9 mmol as the content was regarded as 60%) was added at room temperature. The mixture was stirred at room temperature for 15 minutes in a nitrogen atmosphere. To the mixture, 4-chloro-2,3-dimethylpyridine 1-oxide (3.03 g, 19.2 mmol) was added, and the mixture was stirred at 60° C. for 3 hours and 20 minutes. After cooled to room temperature, the reaction mixture was concentrated. The residue was purified by silica gel column chromatography (NH silica gel: 250 g, elution solvent: ethyl acetate, ethyl acetate/methanol=10/1) to obtain the title compound (3.84 g, yield: 74.8%) as a pale brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124780B2
Source datasetuspto-grants-2012_02
ORD IDord-16081400f26f455aa2df0a8372bd4c63
Source noteuspto-grants-2012_02