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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl mercaptanHCID 7509—
ReactantSodium hydrideHCID 24758—
Reactant2-Bromo-3-methylpyridineHCID 220832—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product3-Methyl-2-(phenylmethylthio)-pyridineHCID 14653187222.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969387B2
Source datasetuspto-grants-2015_03
ORD IDord-17ca926e5c5546ab8baea1c670c08659
Source noteuspto-grants-2015_03