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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 259351Erstellt: 25. Oktober 2026

Butyl bromide → 9-(p-Vinylphenyl)acridine

https://huagongshe.com/reaction/259351

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktButyl bromideHCID 8002—
EduktLithiumHCID 3028194—
Eduktp-IODOSTYRENEHCID 11009755—
Edukt9-BromoacridineHCID 15588290—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelCobalt(II) chlorideHCID 24288—
Produkt9-(p-Vinylphenyl)acridineHCID 2276087038,5%

Reaktionsschritte

A solution of butyl lithium in ether was obtained by reacting a solution consisting of 137 g of butyl bromide and 200 ml of ether with a suspension consisting of 17 g of lithium and 400 ml of ether by the use of the same apparatus as that used in Referential Example 1. This solution was added dropwise to 300 ml of an ether solution containing 180 g of 9-bromoacridine at 0°-5° C., and the mixture was then warmed gradually to room temperature and stirred for further 3 hours. To the mixture was added dropwise 322 g of p-iodostyrene diluted with 300 ml of ether in the presence of cobalt chloride with stirring in a nitrogen gas stream, and the mixture was then refluxed for 5 hours. The reaction mixture was poured onto hydrochloric acid-ice and stirred. The organic layer was extracted with ether, and the extract was dried over anhydrous sodium sulfate. The solvent was then distilled off to obtain yellowish white crystals. The crystals were purified by alumina column chromatography to obtain 75.6 g of 9-(p-vinylphenyl)acridine, yield 38.4%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04037036
Quelldatensatzuspto-grants-1977_07
ORD IDord-61e0860a733c48b68bc234dcf88a7e7a
Quellennotizuspto-grants-1977_07