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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 869756Generated: October 31, 2026

Benzyl mercaptan → 2-(Benzylthio)-5-methoxypyridine

https://huagongshe.com/reaction/869756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl mercaptanHCID 7509—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Bromo-5-methoxypyridineHCID 11148151—
Catalyst1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
Product2-(Benzylthio)-5-methoxypyridineHCID 58349831105.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 2-bromo-5-methoxypyridine (1.13 g) in toluene (15 mL) were added phenylmethanethiol (820 mg), N,N-diisopropylethylamine (1.71 g), tris(dibenzylideneacetone)dipalladium(0) (220 mg) and 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (278 mg), and the mixture was stirred under an argon atmosphere at 80° C. for 3 hr. The reaction mixture was filtered through silica gel, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent:hexane-ethyl acetate=49:1→19:1) to give the title compound as a yellow oil (yield 1.47 g, quantitative).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969387B2
Source datasetuspto-grants-2015_03
ORD IDord-1a327cc8b118479b8d5a937581b38461
Source noteuspto-grants-2015_03