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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 402292Erstellt: 25. Oktober 2026

Water → 3-Methyl-4-[((4-methyl-1-propylimidazol-5-yl)methyl)sulfanyl]aniline

https://huagongshe.com/reaction/402292

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktTriethylamineHCID 8471—
Edukt4-Amino-2-methylbenzene-1-thiolHCID 19867385—
Edukt5-Chloromethyl-4-methyl-1-propylimidazole hydrochlorideHCID 22938550—
LösungsmittelMethanolHCID 887—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-Methyl-4-[((4-methyl-1-propylimidazol-5-yl)methyl)sulfanyl]anilineHCID 6865009330,4%

Reaktionsschritte

To a solution of 4-amino-2-methylthiophenol (500 mg) and triethylamine (3.0 ml) in tetrahydrofuran (15 ml) was added dropwise a solution of 5-chloromethyl-4-methyl-1-propylimidazole hydrochloride (908 mg) in methanol (5 ml) at 0° C. under argon atmosphere, after which the mixture was returned to room temperature and stirred for 3 hours. Water was added and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine and dried with magnesium sulfate. The solvent was distilled off under reduced pressure, and the resulting residue was purified by basic silica gel column chromatography (hexane:ethyl acetate=1:1→ethyl acetate) to give 3-methyl-4-[((4-methyl-1-propylimidazol-5-yl)methyl)sulfanyl]aniline (301 mg) as a brown powder.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08741943B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-eb87a8ccc5984ecd8effc4155f02d4ad
Quellennotizuspto-grants-2014_06