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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1623581Generated: October 31, 2026

1-Butanol → HCID 68467290, compound

https://huagongshe.com/reaction/1623581

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-ButanolHCID 263—
ReactantSodium hydrideHCID 24758—
Reactant4-Chloro-2,3-dimethyl-1-oxidopyridin-1-iumHCID 9877446—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductHCID 68467290HCID 6846729096.4%

Reaction Conditions

Temperature30 °C

Reaction Steps

To a solution prepared by diluting 8.6 g (2.0 eq.) of 60% sodium hydride with 200 mL of dimethylsulfoxide, 16.0 g (2.0 eq.) of 1-butanol was added, and the mixture was allowed to react for one hour at 60° C. The reaction liquid was cooled to 30° C., and then a liquid containing 17.0 g of 4-chlor-2,3-dimethylpyridine-1-oxide dissolved in dimethylsulfoxide (70 mL) was added dropwise. The mixture was allowed to react for 3 hours at 40 to 50° C., and was left to stand overnight at room temperature. 15 mL of water was added to the reaction liquid, and the mixture was concentrated, to obtain a residue in the form of a black paste. Subsequently, the residue was dissolved in 500 mL of water, and then the aqueous solution was extracted three times with 670 mL of chloroform. The extract was dried over anhydrous magnesium sulfate, and was concentrated to dryness under reduced pressure. The obtained residue was purified on a silica gel column, to obtain 20.3 g of 4-butoxy-2,3-dimethylpyridine-1-oxide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778975B2
Source datasetuspto-grants-2014_07
ORD IDord-1ae6ecb7c4cb43cd9374e5f24f033eef
Source noteuspto-grants-2014_07