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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2047903Erstellt: 27. Oktober 2026

Benzyl mercaptan → 2-(Benzylthio)-4-methylpyridine

https://huagongshe.com/reaction/2047903

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl mercaptanHCID 7509—
EduktSodium hydrideHCID 24758—
Edukt2-Bromo-4-methylpyridineHCID 2734087—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-(Benzylthio)-4-methylpyridineHCID 5834983656%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

To a suspension of sodium hydride (60% in oil, 512 mg) in tetrahydrofuran (45 mL) was added dropwise phenylmethanethiol (1.52 g) at room temperature, 2-bromo-4-methylpyridine (2.0 g) was added, and the mixture was stirred at 60° C. for 72 hr. The reaction mixture was diluted with water and 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=24:1) to give the title compound as a brown oil (yield 1.40 g, 56%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08592597B2
Quelldatensatzuspto-grants-2013_11
ORD IDord-e47eb8bc3e1a4336acf77c01ad0635f5
Quellennotizuspto-grants-2013_11