HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 869739Generated: October 26, 2026
Benzyl mercaptan → 3-Methyl-2-(phenylmethylthio)-pyridine
https://huagongshe.com/reaction/869739
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl mercaptan | HCID 7509 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Bromo-3-methylpyridine | HCID 220832 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Methyl-2-(phenylmethylthio)-pyridine | HCID 14653187 | 222.1% |
Reaction Steps
To a suspension of sodium hydride (60% in oil, 1.44 g) in tetrahydrofuran (45 mL) was added dropwise phenylmethanethiol (465 mg) at room temperature and the mixture was stirred for 15 min. 2-Bromo-3-methylpyridine (2.0 g) was added to the reaction mixture, and the mixture was stirred at 60° C. for 1.5 hr. The reaction mixture was diluted with water, and concentrated under reduced pressure. The residual aqueous layer was extracted twice with ethyl acetate. Combined organic layers were washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent:hexane-hexane-ethyl acetate=97:3) to give the title compound as a gray oil (yield 1.79 g, 72%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08969387B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-17ca926e5c5546ab8baea1c670c08659 |
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| Source note | uspto-grants-2015_03 |
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