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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223296Generated: October 29, 2026

Toluene → HCID 178494250, compound

https://huagongshe.com/reaction/223296

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 13374347HCID 13374347—
SolventMethanolHCID 887—
ProductHCID 178494250HCID 17849425059%

Reaction Steps

A solution of 13.25 ml (0.0581 m) of 25% sodium methoxide in methanol was added dropwise to a mixture of 20 g (0.063 m) of 2-chloro-4-benzyloxy-5-[(6-methyl-3-pyridinyl)-methyl]-pyrimidine prepared as in Example 3 and 250 ml of toluene. The mixture is allowed to stir overnight at room temperature then washed with water and evaporated. The residual oil which was 2-methoxy-4-benzyloxy-5-[(6-methyl-3-pyridinyl)-methyl]-pyrimidine was dissolved in ethanol and hydrogenated over 0.6 g of 10% palladium on charcoal. After hydrogen absorption, the reaction mixture was filtered, concentrated to an oil which was taken up in methylene dichloride. Ether was added to give 8.4 g (59%) of 2-methoxy-5-[(6-methyl-3-pyridinyl)-methyl]-4-(1H)-pyrimidinone, m.p. 145°-147°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04352933
Source datasetuspto-grants-1982_10
ORD IDord-f99cc1cd12904ba28f5759297bc543a3
Source noteuspto-grants-1982_10