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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1504385Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/1504385

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl mercaptanHCID 7509—
Edukt1,4-DioxaneHCID 31275—
Edukt4-Bromo-2-nitroanilineHCID 70132—
EduktDiisopropylethylamineHCID 81531—
Katalysator1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
LösungsmittelWaterHCID 962—
Produkt4-(Benzylthio)-2-nitroanilineHCID 1355099388,2%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A screw cap vial was charged with 4-bromo-2-nitroaniline (7.00 g, 32.3 mmol), xantphos (0.933 g, 1.613 mmol), tris(dibenzylideneacetone)dipalladium (0) (0.738 g, 0.806 mmol), 1,4-Dioxane (32.3 ml), and DIPEA (11.22 ml, 64.5 mmol). The vial was purged with Argon, sealed and heated to 80° C. for 10 minutes. The reaction was cooled to room temperature and benzyl mercaptan (4.01 ml, 33.9 mmol) was added and the reaction heated at 80° C. for 3 hours. The reaction was cooled to room temperature, diluted with water and extracted with DCM (3×). The combined organics were washed with water and brine, dried over magnesium sulfate, filtered and concentrated. The resulting material was concentrated, dissolved in minimal DCM and purified via column chromatography (silica gel 40 g, gradient elution 0 to 50% EtOAc:Heptane) to afford 4-(benzylthio)-2-nitroaniline (7.43 g, 28.5 mmol, 88% yield). m/z (ESI) 261.2 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09212182B2
Quelldatensatzuspto-grants-2015_12
ORD IDord-1e006f5cddc94ebfac893136c2591d2d
Quellennotizuspto-grants-2015_12