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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1811778Generated: November 2, 2026

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

https://huagongshe.com/reaction/1811778

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 numberUS08362241B2
Source datasetuspto-grants-2013_01
ORD IDord-c8f502093d7e4b89971c917091248a58
Source noteuspto-grants-2013_01