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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1759970Generated: October 28, 2026

Methyl iodide → HCID 22599805, compound

https://huagongshe.com/reaction/1759970

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 22599669HCID 22599669—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22599805HCID 22599805—

Reaction Steps

In 3 ml of tetrahydrofuran was suspended 0.08 g of sodium hydride (60% in oil), to which 6-methylthio-4-(α-hydroxylbenzyl)pyrimidine dissolved in 0.3 ml of tetrahydrofuran was added. The mixture was stirred at 0° C. for 15 minutes, to which 0.28 g of iodomethane was added dropwise at room temperature, followed by stirring at the same temperature for 30 minutes. The reaction mixture was then poured into a saturated aqueous ammonium chloride solution and extracted three times with ethyl acetate. The organic layers were combined, washed with water, dried over anhydrous magnesium sulfate, and then concentrated. The residue was subjected to silica gel column chromatography to give 0.17 g of 6-methylthio-4-(α-methoxybenzyl)pyrimidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06838463B2
Source datasetuspto-grants-2005_01
ORD IDord-2686dc7358f3402d8641adde9ca7fac7
Source noteuspto-grants-2005_01