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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2238640Generated: October 31, 2026

Sodium Hydroxide → 4-Chloro-6-methyl-2-(methylthio)pyrimidine

https://huagongshe.com/reaction/2238640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant4-Chloro-2-methylthiopyrimidineHCID 97113—
Reactant4,5-Dichloro-3,6-dihydroxybenzene-1,2-dicarbonitrileHCID 299493—
ReactantHCID 178418348HCID 178418348—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product4-Chloro-6-methyl-2-(methylthio)pyrimidineHCID 241163—

Reaction Conditions

Temperature0 °C

Reaction Steps

5.93 mL of 4-chloro-2-methylthiopyrimidine was dissolved in 50 mL of diethyl ether, and 100 mL of methyllithium (1M diethyl ether solution) was gradually added to the solution at −78° C. The reaction solution was stirred at 0° C. for 1 hour, and then a solution prepared by mixing 2.3 mL of water and 15 mL of tetrahydrofuran was added thereto. The reaction solution was stirred at the same temperature for 10 minutes, and then 50 mL of a tetrahydrofuran solution containing 13.7 g of 2,3-dichloro-5,6-dicyanohydroquinone was added thereto. The reaction solution was stirred at the same temperature for 1 hour, and then 100 mL of a 1 N aqueous solution of sodium hydroxide was added to the reaction solution. The obtained reaction solution was extracted with hexane, and the organic layer was washed with a 1 N aqueous solution of sodium hydroxide and saturated brine. After drying over anhydrous magnesium sulfate, the insolubles were filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography to obtain 5.1 g of 4-chloro-6-methyl-2-(methylthio)pyrimidine [42-1] as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07718801B2
Source datasetuspto-grants-2010_05
ORD IDord-39fce71304e840cbb295239ee7b72f8b
Source noteuspto-grants-2010_05