HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2285524Generated: November 1, 2026
Hydrochloric Acid → HCID 178493772, compound
https://huagongshe.com/reaction/2285524
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methyl formate | HCID 7865 | — |
| Reactant | Methyl methoxyacetate | HCID 80507 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 2-Methylsulfanyl-acetamidine hydrochloride | HCID 20157976 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178493772 | HCID 178493772 | 70% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04323571 |
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| Source dataset | uspto-grants-1982_04 |
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| ORD ID | ord-970ef07b3b504b8793a7a9b5d6c4b889 |
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| Source note | uspto-grants-1982_04 |
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