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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580316Generated: November 1, 2026

4,4-Dimethoxy-2-butanone → HCID 14253092, compound

https://huagongshe.com/reaction/580316

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,4-Dimethoxy-2-butanoneHCID 228548—
ReactantSodium ethoxideHCID 2723922—
ReactantSodiumHCID 5360545—
ReactantHCID 14253091HCID 14253091—
SolventAcetic AcidHCID 176—
SolventAcetoneHCID 180—
SolventEthanolHCID 702—
SolventHexaneHCID 8058—
ProductHCID 14253092HCID 1425309268%

Reaction Steps

To 6-n-butyl-2-picoline amidine hydrochloride (3 g) were added sodium ethoxide solution in ethanol prepared from ethanol (100 ml) and metallic sodium (0.65 g) and then 1,1-dimethoxy-3-butanone (purity 90 %, 2.16 g). The mixture was heated under refluxing for three hours, and was left to stand at room temperature. After acetic acid was added into the mixture to be weak acidic condition, the mixture was concentrated under reduced pressure. The residue was dissolved in chloroform (200 ml), followed by washing with water (50 ml) and drying over anhydrous magnesium sulfate and concentration under reduced pressure. The residue obtained was subjected to silica gel column chromatography (eluent; hexane:acetone=2:1) to obtain 2-(6-n-butyl-2-pyridinyl)-4-methylpyrimidine (2.17 g, yield: 68 %).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04752608
Source datasetuspto-grants-1988_06
ORD IDord-f967e3caf01a43ad8850bf1de6e90e14
Source noteuspto-grants-1988_06