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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1810801Generated: October 26, 2026

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

https://huagongshe.com/reaction/1810801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant4-Amino-2-methylbenzene-1-thiolHCID 19867385—
Reactant5-(chloromethyl)-1-propyl-1H-imidazole hydrochlorideHCID 22938616—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product3-Methyl-4-(((1-propylimidazol-5-yl)methyl)sulfanyl)anilineHCID 6615438264%

Reaction Steps

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-1-propylimidazole hydrochloride (847 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, and 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) and was recrystallized from hexane-ethyl acetate to give 3-methyl-4-[((1-propylimidazol-5-yl)methyl)sulfanyl]aniline (601 mg) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362058B2
Source datasetuspto-grants-2013_01
ORD IDord-cda5409276ef48f8a6c95ff1a14f9ea6
Source noteuspto-grants-2013_01