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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 347352Erstellt: 25. Oktober 2026

Water → 4-acetyl-N-(tert-butyldimethylsiloxy)benzenesulfonamide

https://huagongshe.com/reaction/347352

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktTriethylamineHCID 8471—
Edukt4-Acetylbenzenesulfonyl chlorideHCID 266418—
EduktO-(tert-Butyldimethylsilyl)hydroxylamineHCID 4691350—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-acetyl-N-(tert-butyldimethylsiloxy)benzenesulfonamideHCID 2108252878,9%

Reaktionsschritte

Ex-33A: To a solution of O-(tert-butyldimethylsilyl)hydroxylamine (0.74 g, 5 mmol) and triethylamine (1.01 g, 10 mmol) in 25 ml THF, 4-acetylbenzenesulfonyl chloride(1.1 g, 5 mmol) was added at 0° C. The mixture was stirred overnight and then poured into H2O. The precipitate was filtered, dried, and recrystallized from EtOAc/Hexene to give 1.3 g (76.8%) of 4-acetyl-N-(tert-butyldimethylsiloxy)benzenesulfonamide as a white solid. 1H-NMR (300 MHz, CDCl3) δ 8.11 (d, J=9 Hz, 2H), 8.01 (d, J=9 Hz, 2H), 6.59 (b, 1H), 2.67 (s, 3H), 0.89 (s, 9H), 0.20 (s, 6H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07173129B2
Quelldatensatzuspto-grants-2007_02
ORD IDord-8405d919c0c34009802b017a6c56ebd7
Quellennotizuspto-grants-2007_02