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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1503084Erstellt: 25. Oktober 2026

2-Methoxyaniline → 4-methoxy-N-(2-methoxyphenyl)benzenesulfonamide

https://huagongshe.com/reaction/1503084

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-MethoxyanilineHCID 7000—
Edukt4-Methoxybenzenesulfonyl chlorideHCID 7401—
EduktTriethylamineHCID 8471—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-methoxy-N-(2-methoxyphenyl)benzenesulfonamideHCID 74341775,3%

Reaktionsschritte

To a solution of 4-methoxybenzenesulfonyl chloride (5.0 g, 24 mmol) and 2-methoxyaniline (3.0 g, 24 mmol) in dichloromethane (24 mL) at 0° C. was added triethylamine (3.4 mL, 24 mmol) over 10 minutes. The ice bath was removed, and the mixture was stirred for 16 hr. The mixture was diluted with dichloromethane (100 mL) and the combined solution was washed with water (50 mL) and brine (50 mL). The organic solution was dried over MgSO4, filtered, and evaporated, and the crude product was purified by silica gel chromatography (15-60% EtOAc/Hex). Product-containing fractions were pooled, evaporated, and dried under high vacuum to yield 5.3 g (44%) of the product as a tan-colored oil: 1H-NMR (CDCl3) δ 7.70-7.67 (d, 2H), 7.53-7.50 (d, 1H), 7.05-6.99 (m, 2H), 6.91-6.83 (m, 3H), 6.73 (d, 1H), 3.80 (s, 3H), 3.65 (s, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09212134B2
Quelldatensatzuspto-grants-2015_12
ORD IDord-27558dc9d9c345b6819f96b64c294c61
Quellennotizuspto-grants-2015_12