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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 640658Erstellt: 23. Oktober 2026

Acetic Anhydride → N-(3-bromobenzenesulfonyl)acetamide

https://huagongshe.com/de/reaction/640658

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AnhydrideHCID 7918—
Edukt3-Bromobenzene-1-sulfonamideHCID 2734765—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelPyridineHCID 1049—
LösungsmittelEthyl AcetateHCID 8857—
ProduktN-(3-bromobenzenesulfonyl)acetamideHCID 6121623351%

Reaktionsschritte

3-Bromobenzenesulfonamide (470 mg, 2.0 mmol) was dissolved in pyridine (1 mL). To this solution was added DMAP (7.3 mg, 0.060 mmol) and then acetic anhydride (570 μL, 6.0 mmol). The reaction was stirred for 3 h at room temperature during which time the reaction changed from a yellow solution to a clear solution. The solution was diluted with ethyl acetate, and then washed with aqueous NH4Cl solution (×3) and water. The organic layer was dried over MgSO4 and concentrated. The resulting oil was triturated with hexanes and the precipitate was collected by filtration to obtain N-(3-bromophenylsulfonyl)-acetamide as a shiny white solid (280 mg, 51%). 1H NMR (400 MHz, DMSO-d6) δ 12.43 (s, 1H), 8.01 (t, J=1.8 Hz, 1H), 7.96-7.90 (m, 2H), 7.61 (t, J=8.0 Hz, 1H), 1.95 (s, 3H); HPLC ret. time 1.06 min; ESI-MS 278.1 m/z (MH+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07691902B2
Quelldatensatzuspto-grants-2010_04
ORD IDord-adcbb3d0e03e4f6cbd2417b97bb44d7c
Quellennotizuspto-grants-2010_04