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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 61316Erstellt: 24. Oktober 2026

Nitrogen → HCID 12670251, Verbindung

https://huagongshe.com/de/reaction/61316

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNitrogenHCID 947—
EduktAzobisisobutyronitrileHCID 6547—
EduktN-bromobutanimideHCID 67184—
Edukt7-Bromobicyclo[4.2.0]octa-1,3,5-trieneHCID 568591—
LösungsmittelChlorobenzeneHCID 7964—
ProduktHCID 12670251HCID 1267025193%

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

Bromobenzocyclobutene (91.5 g, 0.5 mol) and chlorobenzene(anhydrous, 2500 mL) were charged into a four-neck 5 L flask equipped with mechanical stir, condenser, N2 (in and outlet) and thermometer. The reaction mixture was heated to 120° C., and N-bromosuccinimide (111.3 g, 0.625 mol) was gradually charged over 30 min., followed by slowly feeding a mixture of a free radical azo compound source (VAZO™ 68) (14.0 g, 0.05 mol) and chlorobenzene (500 mL) over 30 min. Then the reaction mixture was heated to 133° C. (mild reflux) and kept at that temperature for 6 hr. The mixture was then cooled to room temperature overnight, and chlorobenzene was removed by vacuum evaporation. The crude product was extracted with hexane. After removal of hexane, 1-bromo-bromobenzocyclobutene (1-Br-BrBCB) (80-85° C/0.35 torr, 90 g, ca. 93% purity) was obtained by vacuum distillation.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09441055B1
Quelldatensatzuspto-grants-2016_09
ORD IDord-3899512d2f51492bb1b2c07fddff8478
Quellennotizuspto-grants-2016_09