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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4,4-Dimethoxy-2-butanone | HCID 228548 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 14253091 | HCID 14253091 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 14253092 | HCID 14253092 | 68% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04752608 |
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| Source dataset | uspto-grants-1988_06 |
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| ORD ID | ord-f967e3caf01a43ad8850bf1de6e90e14 |
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| Source note | uspto-grants-1988_06 |
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