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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 453519Erstellt: 24. Oktober 2026

Benzyltrimethylammonium hydroxide → (Z)-N-(4-chlorophenethyl)-4-(2-bromo-4-(2-(methylsulfinyl)-2-(methylthio)vinyl)phenoxy)benzamide

https://huagongshe.com/de/reaction/453519

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyltrimethylammonium hydroxideHCID 66854—
EduktMethyl (methylsulfinyl)methyl sulfideHCID 99129—
EduktN-(4-chlorophenethyl)-4-(2-bromo-4-formylphenoxy)benzamideHCID 86643286—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(Z)-N-(4-chlorophenethyl)-4-(2-bromo-4-(2-(methylsulfinyl)-2-(methylthio)vinyl)phenoxy)benzamideHCID 8664328796,1%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

N-(4-chlorophenethyl)-4-(2-bromo-4-formylphenoxy)benzamide (1.6 g, 3.5 mmol) was diluted with THF (10 mL) followed by the addition of N,N,N-trimethyl(phenyl)methanaminium hydroxide (0.79 ml, 1.7 mmol) and methylsulfinyl (methylthio)methane (0.87 g, 7.0 mmol). The reaction was stirred at 70° C. for 2 hours. The reaction mixture was loaded directly onto a silica gel column and eluted with DCM:MeOH (98:2) to yield (Z)—N-(4-chlorophenethyl)-4-(2-bromo-4-(2-(methylsulfinyl)-2-(methylthio) vinyl)phenoxy)benzamide (1.9 g, 96% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08492437B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-558783616cce47f3bf0a9cc5418151ff
Quellennotizuspto-grants-2013_07