HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402291Generated: October 26, 2026
Water → 3-Methyl-4-(((1-propylimidazol-5-yl)methyl)sulfanyl)aniline
https://huagongshe.com/reaction/402291
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Amino-2-methylbenzene-1-thiol | HCID 19867385 | — |
| Reactant | 5-(chloromethyl)-1-propyl-1H-imidazole hydrochloride | HCID 22938616 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Methyl-4-(((1-propylimidazol-5-yl)methyl)sulfanyl)aniline | HCID 66154382 | 64% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08741943B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-715fbd2a0c74464aa862e5afd37ae5d6 |
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| Source note | uspto-grants-2014_06 |
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