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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1621366Generated: October 26, 2026

Sodium methanethiolate → 2-Methyl-4-(methylthio)-6-(tributylstannyl)pyrimidine

https://huagongshe.com/reaction/1621366

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium methanethiolateHCID 4378561—
Reactant4-Chloro-2-methyl-6-(tributylstannyl)pyrimidineHCID 86647045—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-Methyl-4-(methylthio)-6-(tributylstannyl)pyrimidineHCID 5954828030%

Reaction Steps

Sodium thiomethoxide (140 mg, 2 mmol) was added to 4-chloro-2-methyl-6-(tributylstannyl)pyrimidine (835 mg, 2 mmol) in tetrahydrofuran (10 mL). The reaction mixture was stirred at room temperature for 48 h. The reaction mixture was diluted with water (20 mL) and extracted with EtOAc (2×30 mL). The organic extract was washed with saturated NaCl (5 mL) and dried over Na2SO4. The solution was filtered and concentrated in vacuo to give the crude material as an orange oil. The crude product was purified by silica gel chromatography, eluting with 5% EtOAc/hexanes to give 2-methyl-4-(methylthio)-6-(tributylstannyl)pyrimidine (256 mg, 30% yield). 1H NMR (300 MHz, CDCl3) δ 7.07 (s, 1H); 2.62 (s, 3H); 2.51 (s, 3H); 1.44-1.70 (m, 6H); 1.21-1.42 (m, 6H); 0.98-1.21 (m, 6H); 0.91 (t, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772480B2
Source datasetuspto-grants-2014_07
ORD IDord-34fb1bcf92a2488fbce1d10539186773
Source noteuspto-grants-2014_07