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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 501881Generated: October 25, 2026

Tert-Butyl hypochlorite → 2-[(4,6-Dimethoxypyrimidin-2-yl)-methylthiomethyl]-6-methoxymethylaniline

https://huagongshe.com/reaction/501881

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-Butyl hypochloriteHCID 521297—
ReactantSodium MethoxideHCID 10942334—
Reactant2-(Methoxymethyl)anilineHCID 12334306—
Reactant2-Methylthiomethyl-4,6-dimethoxypyrimidineHCID 57428123—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product2-[(4,6-Dimethoxypyrimidin-2-yl)-methylthiomethyl]-6-methoxymethylanilineHCID 1672631458.8%

Reaction Conditions

Temperature-70 °C

Reaction Steps

2-Methoxymethylaniline (0.68 g, 4.96 mmol) was dissolved in dichloromethane (50 ml) and the solution was cooled to −70° C. To the cooled solution a solution of tert-butyl hypochlorite (0.54 g, 4.96 mmol) in dichloromethane (1 ml) was added dropwise and the solution was stirred at −70° C. for 10 minutes. To the obtained reaction solution a solution of 2-methylthiomethyl-4,6-dimethoxypyrimidine (0.893 g, 4.46 mmol) in dichloromethane (5 ml) was added dropwise and the solution was stirred at −70° C. for 30 minutes. To the obtained reaction solution a 28% methanol solution of sodium methoxide (4 ml) was added and the solution was stirred until its temperature reached room temperature. Water was added to the reaction solution and the organic layer was separated. The water layer was further extracted twice with dichloromethane. The organic layer was washed with water and dried. Then dichloromethane was distilled off under reduced pressure and the obtained oily substance was purified by column chromatography using 1:6 mixed solvent of ethyl acetate and hexane as eluent to obtain 2-[(4,6-dimethoxypyrimidin-2-yl)-methylthiomethyl]-6-methoxymethylaniline (0.88 g, yield 53%) as oily substance;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772395B2
Source datasetuspto-grants-2010_08
ORD IDord-8f4ca55198c64fdfb6527531970c3dc7
Source noteuspto-grants-2010_08