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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2285524Generated: November 1, 2026

Hydrochloric Acid → HCID 178493772, compound

https://huagongshe.com/reaction/2285524

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl formateHCID 7865—
ReactantMethyl methoxyacetateHCID 80507—
ReactantSodium MethoxideHCID 10942334—
Reactant2-Methylsulfanyl-acetamidine hydrochlorideHCID 20157976—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 178493772HCID 17849377270%

Reaction Steps

5.4 g (0.1 mol) of solid sodium methylate were added in portions to a mixture of 10.4 g (0.1 mol) of methoxyacetic acid methyl ester and 6 g (0.1 mol) of formic acid methyl ester at 20°-25° C. and the mixture was subsequently stirred at room temperature for 5 hours. A further 5.4 g (0.1 mol) of sodium methylate, dissolved in 40 ml of methanol, were then added, 14.1 g (0.1 mol) of methylthioacetamidine hydrochloride were subsequently added to the mixture and the mixture was then stirred at room temperature for 24 hours. The solvent was now stripped off in vacuo, the residue was dissolved in 300 ml of water and the solution was brought to pH 6 by adding concentrated hydrochloric acid. The solution was then twice extracted by shaking with 150 ml of methylene chloride each time, the organic phase was dried over sodium sulphate and the solvent was distilled off in vacuo. 13 g (70% of theory) of 2-methylthiomethyl-6-hydroxy-5-methoxypyrimidine were obtained in this manner in the form of a light brown powder with a melting point of 102° C. ##STR9##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04323571
Source datasetuspto-grants-1982_04
ORD IDord-970ef07b3b504b8793a7a9b5d6c4b889
Source noteuspto-grants-1982_04