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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 625896Erstellt: 24. Oktober 2026

Azobisisobutyronitrile → HCID 90238913, Verbindung

https://huagongshe.com/de/reaction/625896

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAzobisisobutyronitrileHCID 6547—
EduktTriethylamineHCID 8471—
EduktN-bromobutanimideHCID 67184—
Edukt6-Chloro-1-indanoneHCID 5100705—
Lösungsmittel1,2-DichloroethaneHCID 11—
LösungsmittelWaterHCID 962—
ProduktHCID 90238913HCID 90238913—

Reaktionsschritte

To a solution of 6-chloro-1-indanone (II) (100.0 g, 600.2 mmol) in 1,2-dichloroethane (1.00 L) was added 2,2′-azo-bis-isobutyronitrile (9.86 g, 60.0 mmol) followed by N-bromosuccinimide (224.3 g, 1.26 mol). The reaction mixture was quickly heated to reflux. After 30 min at reflux, more 2,2′-azo-bis-isobutyronitrile (9.86 g, 60.0 mmol) was added. The reaction mixture was kept for 4.5 h at reflux. Afterwards the mixture was stirred at room temperature overnight. The mixture was cooled to 0° C., and triethylamine (126 mL, 904 mmol) was added dropwise. The mixture was stirred for 1 h at 0° C., and then allowed to heat to room temperature. Water (1.0 L) was added. The mixture was vigorously stirred for 15 min. The stirring was stopped, and the aqueous layer was removed by suction. Fresh water (1.0 L) was added, and the mixture was stirred for 15 min. The aqueous layer was then separated by suction. The organic phase was further shaken with brine (500 mL) in a separating funnel.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09309165B2
Quelldatensatzuspto-grants-2016_04
ORD IDord-26fc7dc60172410ab7deafcb0da71c26
Quellennotizuspto-grants-2016_04