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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1525656Erstellt: 26. Oktober 2026

N-bromobutanimide → 4-(Bromomethyl)-N-[(dimethylamino)sulfonyl]-2,5-difluorobenzamide

https://huagongshe.com/reaction/1525656

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-bromobutanimideHCID 67184—
EduktN-[(Dimethylamino)sulfonyl]-2,5-difluoro-4-methylbenzamideHCID 89619137—
KatalysatorAzobisisobutyronitrileHCID 6547—
Lösungsmittel1,2-DichloroethaneHCID 11—
Produkt4-(Bromomethyl)-N-[(dimethylamino)sulfonyl]-2,5-difluorobenzamideHCID 89619586—

Reaktionsschritte

A mixture of N-[(dimethylamino)sulfonyl]-2,5-difluoro-4-methylbenzamide (Preparation 2, 0.50 g, 1.80 mmol), N-bromosuccinimide (freshly recrystallised and dried, 0.42 g, 2.34 mmol) and azobisisobutyronitrile (14.8 mg, 0.09 mmol) in 1,2-dichloroethane (15 mL) was heated under reflux with stirring whilst being irradiated with light from a 100 watt lamp. After 6 hours more N-bromosuccinimide (300 mg, 1.69 mmol) and azobisisobutyronitrile (10 mg, 0.06 mmol) were added and the mixture heated for a further 4 hours. An additional amount of N-bromosuccinimide (100 mg, 0.56 mmol) was then added and the mixture heated under reflux for a further 4 hours. The reaction mixture was cooled to room temperature and evaporated in vacuo to leave a pale yellow oil (0.54 g). Purification by silica gel column chromatography eluting with ethyl acetate/heptane 0:100-1:4 afforded the title compound (0.176 g, 27%) as a colourless oil which solidified on standing.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09085517B2
Quelldatensatzuspto-grants-2015_07
ORD IDord-1ddd56819010476e86f10678abc041c8
Quellennotizuspto-grants-2015_07