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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2231646Generated: November 1, 2026

Sulfuric Acid → HCID 14281075, compound

https://huagongshe.com/reaction/2231646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium CarbonateHCID 10340—
ReactantSodium HydroxideHCID 14798—
ReactantSodium hydrideHCID 24758—
Reactant2,2-DiethylpropanedioateHCID 6951563—
ReactantHCID 14281141HCID 14281141—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14281075HCID 1428107586.3%

Reaction Steps

To tetrahydrofuran (30 ml) were added diethylmalonate (1.6 g) and 60% oily sodium hydride (0.4 g), and then 4-chloro-6-methyl-2-(6-phenyl-2-pyridinyl)pyrimidine (2 g). The mixture was heated under refluxing for 30 minutes. Sodium hydroxide (0.85 g) solution in water (10 ml) and methanol (10 ml) was added thereto, and the mixture was further heated under refluxing for 20 minutes. After the mixture was left to stand until it was cooled to room temperature, sulfuric acid (1.4 g) was added dropwise thereto. The mixture was heated under refluxing for 30 minutes and left to stand to room temperature. 1-N aqueous sodium carbonate solution was added until a mixture was neutralized, and concentrated under reduced pressure. The residue was subjected to silica-gel column chromatography (eluent; n-hexane:acetone=3:1 in volume) to give 4,6-dimethyl-2-(6-phenyl-2-pyridinyl)pyrimidine (1.6 g, yield 86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04783466
Source datasetuspto-grants-1988_11
ORD IDord-01006dce3f57465e90557d5acab9a50d
Source noteuspto-grants-1988_11