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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 553471Erstellt: 24. Oktober 2026

Sodium Carbonate → 2-(2-sulfamoylphenoxy)-N-methylacetamide

https://huagongshe.com/de/reaction/553471

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium CarbonateHCID 10340—
EduktCesium carbonateHCID 10796—
EduktPotassium CarbonateHCID 11430—
EduktSodium BicarbonateHCID 516892—
EduktPotassium BicarbonateHCID 516893—
Edukt2-Hydroxybenzene-1-sulfonamideHCID 637546—
Edukt2-Bromo-N-methylacetamideHCID 15490745—
Produkt2-(2-sulfamoylphenoxy)-N-methylacetamideHCID 57924329—

Reaktionsschritte

2-(2-Sulfamoylphenoxy)-N-methylacetamide can be prepared according to the method of Scheme XXXIX. Bromoacetyl bromide can be reacted methylamine hydrochloride in the presence of a base, such as sodium hydroxide to afford 2-bromo-N-methylacetamide. The phenoxy group of 1-(hydroxy)-2-sulfamoylbenzene can be alkylated with 2-bromo-N-methylacetamide in the presence of a base, such as cesium carbonate, sodium carbonate, potassium carbonate, sodium bicarbonate, potassium bicarbonate, and the like, to afford 2-(2-sulfamoylphenoxy)-N-methylacetamide.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08048862B2
Quelldatensatzuspto-grants-2011_11
ORD IDord-03d8eda5f97b4236b8da1b60fe3c20b6
Quellennotizuspto-grants-2011_11