HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1751176Generated: October 28, 2026
Methyl iodide → 4-(Dimethoxymethyl)-2-(methylsulfanyl)pyrimidine
https://huagongshe.com/reaction/1751176
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | HCID 20716446 | HCID 20716446 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-(Dimethoxymethyl)-2-(methylsulfanyl)pyrimidine | HCID 15407007 | — |
Reaction Steps
Iodomethane (128 g, 902 mmol, 1.20 equiv.) was added carefully to the crude solution of sodium 4-(dimethoxymethyl)pyrimidine-2-thiolate (2) (156 g, 751 mmol) in methanol (700 mL, 1.1 M) while maintaining the reaction temperature below 28° C. using an ice-water bath for cooling. The resulting mixture was stirred at room temperature for 16 h. After removal of the solvent under reduced pressure, the residue was diluted with water (300 mL) and extracted with ethyl acetate (2×150 mL). The combined organic layer was concentrated under reduced pressure and the crude residue purified by passing through a short silica gel pad and washing with diethyl ether (200 mL) to afford 4-(dimethoxymethyl)-2-(methylthio)pyrimidine (3) as a brown oil (53.7 g, 150 g theoretical, 35.7%). LC-MS m/z 201 (M+1). Reference: WO 2006/0097341A1, pg 67.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09157077B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-83aacedfe2fc46ca883534d41fcbae7b |
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| Source note | uspto-grants-2015_10 |
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