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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1810802Generated: October 25, 2026

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

https://huagongshe.com/reaction/1810802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant4-Amino-2-methylbenzene-1-thiolHCID 19867385—
Reactant5-Chloromethyl-4-methyl-1-propylimidazole hydrochlorideHCID 22938550—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product3-Methyl-4-[((4-methyl-1-propylimidazol-5-yl)methyl)sulfanyl]anilineHCID 6865009330.4%

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-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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362058B2
Source datasetuspto-grants-2013_01
ORD IDord-f1bc5ef4b8d04464a7d13fa7b7d44da2
Source noteuspto-grants-2013_01