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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1172020Erstellt: 25. Oktober 2026

1-Bromooctane → 2,6-dibromo-8,9-dihydro-4H-cyclopenta[def]phenanthrene

https://huagongshe.com/reaction/1172020

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-BromooctaneHCID 8140—
EduktSodium HydroxideHCID 14798—
Edukt2,6-dibromo-4H-cyclopenta[def]phenanthreneHCID 59431076—
KatalysatorTetrabutylammonium BromideHCID 74236—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
Produkt2,6-dibromo-8,9-dihydro-4H-cyclopenta[def]phenanthreneHCID 12524367133,6%

Reaktionsschritte

2,6-dibromo-4H-cyclopenta[def]phenanthrene (2.6 g, 7.7 mmol) and octyl bromide (3.6 g, 18.5 mmol) in a 50 ml round bottom flask were dissolved with toluene (10 ml), and tetrabutylammoniumbromide (TBAB) (0.125 g, 0.385 mmol) was added thereto. A solution of NaOH (3.1 g, 77 mmol) in water (50 ml) was added to the reaction mixture, and the resultant solution was refluxed for two days. After the reaction was terminated, the reaction solution was extracted with chloroform. The organic phase was dried over MgSO4, concentrated, and purified by silica gel column chromatography (eluent: n-hexane). The eluate was distilled under a reduced pressure to remove unreacted octyl bromide, thereby giving a compound 2 (3.6 g, 80%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07833635B2
Quelldatensatzuspto-grants-2010_11
ORD IDord-acf87e69a6a146ed983bba7ce1f9e29f
Quellennotizuspto-grants-2010_11