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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043498Generated: October 30, 2026

Methyl iodide → 4-(Dimethoxymethyl)-2-(methylsulfanyl)pyrimidine

https://huagongshe.com/reaction/1043498

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantHCID 20716446HCID 20716446—
SolventMethanolHCID 887—
Product4-(Dimethoxymethyl)-2-(methylsulfanyl)pyrimidineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563539B2
Source datasetuspto-grants-2013_10
ORD IDord-ce7528c250314dcfb647f8ab4052b87c
Source noteuspto-grants-2013_10