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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 523956Erstellt: 26. Oktober 2026

N-bromobutanimide → 5-Bromo-4-amino-2,2-diflouro-1,3-benzodioxole

https://huagongshe.com/reaction/523956

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-bromobutanimideHCID 67184—
Edukt2,2-Difluoro-1,3-dioxaindan-4-amineHCID 2736891—
LösungsmittelDichloromethaneHCID 6344—
Produkt5-Bromo-4-amino-2,2-diflouro-1,3-benzodioxoleHCID 11814311664,2%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a stirred solution of 4-amino-2,2-diflouro-1,3-benzodioxole (2.5 g, 14.4 mmol) in dichloromethane at 0° C. was added N-bromosuccinimide (2.7 g, 15.2 mmol) portion wise. The solution was stirred at 0° C. for 30 min, then at room temperature for 1 h. The reaction mixture was quenched with 1M sodium thiosulfate solution and diluted with deionized water, extracted with dichloromethane (2×50 mL). The combined organic layers were dried (Na2SO4), filtered, and concentrated in vacuo. The crude product was purified by flash chromatography (SiO2, 0-20% ethyl acetate in hexanes) to recover starting material 1 g and afford 5-bromo-4-amino-2,2-diflouro-1,3-benzodioxole as colorless oil (2.33 g, 9.25 mmol, 64%). MS: (ES) m/z calculated for C7H4BrF2NO [M+H]+252.0. found 252.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09340509B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-ca80740c073c413ca1f23ddfff5a55c5
Quellennotizuspto-grants-2016_05