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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 447224Erstellt: 24. Oktober 2026

Chlorobenzene → HCID 10317688, Verbindung

https://huagongshe.com/de/reaction/447224

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChlorobenzeneHCID 7964—
EduktN-bromobutanimideHCID 67184—
EduktN,N-dimethyl-N'-[2-(4-methylphenyl)phenyl]sulfonylmethanimidamideHCID 9972170—
KatalysatorBenzoyl PeroxideHCID 7187—
LösungsmittelWaterHCID 962—
ProduktHCID 10317688HCID 1031768841%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

4′-Methylbiphenyl-2-sulfonic acid 1-dimethylaminometh-(E)-ylideneamide (540.0 mg, 1786 μmol), NBS (318 mg, 1.8 mmol), and benzoyl peroxide (4.3 mg, 17.8 μmol) were dissolved in chlorobenzene (7.0 mL, 69 mmol) and the resulting solution was heated at 100° C. for 90 minutes. The mixture was cooled to room temperature and water was added. The mixture was extracted with DCM, washed with saturated NaHCO3 and saturated aqueous NaCl, extracted again with DCM, dried over MgSO4, filtered, and concentrated. The crude product was purified by flash chromatography (40 g, 0-100% EtOAc in hexanes), then taken up in EtOAc (4.5 mL) and DCM (1.5 mL). Additional DCM (3.0 mL) was added and the mixture was heated at 60° C. The mixture was cooled in the freezer overnight, then concentrated. The material was taken up in DCM (2 mL), EtOAc (6 mL) was added, and the resulting solution placed in the freezer. A precipitate formed and was filtered to yield the title compound (279 mg) as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08481549B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-a0954227e54f42939031ea246f17d11f
Quellennotizuspto-grants-2013_07