HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300995Generated: October 25, 2026
Ethanol → 2-[(2,5-Dimethylphenyl)methylsulfanyl]pyridine
https://huagongshe.com/reaction/2300995
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Benzene, 2-(chloromethyl)-1,4-dimethyl- | HCID 69987 | — |
| Reactant | HCID 178418616 | HCID 178418616 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-[(2,5-Dimethylphenyl)methylsulfanyl]pyridine | HCID 507301 | — |
Reaction Steps
A mixture of 5.6 g (0.05 mole) of 2-mercaptopyridine, 3.3 g (0.05 mole) of potassium hydroxide (85% pellets), 35 ml of ethanol and 5 ml of water was prepared. To this mixture was added 7.8 g (0.05 mole) of 2,5-dimethyl-benzylchloride, while maintaining good stirring. The mixture was stirred and heated to 40° C. for 45 minutes, cooled to room temperature, and then added to 150 ml of water. The aqueous mixture was extracted with 150 ml of diethyl ether; the ether phase washed with 150 ml of water. Finally, the ether phase was dried with anhydrous sodium sulfate. Removal of the ether left a green oil. An infrared spectrum was consistent with the structure of 2-((2,5-dimethylphenyl)methylthio) pyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06498254B1 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-ffe6982de5364bfe97051376edba3789 |
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| Source note | uspto-grants-2002_12 |
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