Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1577469Erstellt: 26. Oktober 2026

Benzene → Bromobutide

https://huagongshe.com/reaction/1577469

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzeneHCID 241—
EduktDicyclohexylcarbodiimideHCID 10868—
EduktCumylamineHCID 68509—
Edukt2-Bromo-3,3-dimethylbutanoic AcidHCID 184251—
LösungsmittelPyridineHCID 1049—
ProduktBromobutideHCID 5307968,8%

Reaktionsschritte

Into a 200 ml four-necked flask, there were charged α-bromo-tert-butylacetic acid (9.8 g) and benzene (50 ml), and pyridine (50 ml) and α,α-dimethylbenzylamine (6.9 g) were dropwise added thereto while stirring at room temperature. Dicyclohexylcarbodiimide (10.8 g) was further added thereto, and the reaction was continued at 60°-70° C. for 6 hours, followed by cooling. The solvent was distilled off under reduced pressure, and the residue was extracted with hot benzene. The benzene extract was concentrated by distillation, and the residue was recrystallized from ethanol to give N-(α,α-dimethylbenzyl)-α-bromo-tert-butylacetamide (10.8 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04288244
Quelldatensatzuspto-grants-1981_09
ORD IDord-f5fd1af2f93548e8849b7c91813b75d6
Quellennotizuspto-grants-1981_09