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HRID 7221Erstellt: 23. Oktober 2026

Hydrogen Bromide → 1,3-Bis(3,5-dibromophenyl)adamantane

https://huagongshe.com/de/reaction/7221

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrogen BromideHCID 260—
Edukt1,3-DibromobenzeneHCID 7927—
EduktBromhydrolHCID 166749—
Edukt1,3-DibromoadamantaneHCID 265790—
Produkt1,3-Bis(3,5-dibromophenyl)adamantaneHCID 22020297194,3%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

After the air inside a 1 litter flask equipped with a thermometer and stirrer was replaced by nitrogen, 43 g of 1,3-dibromoadamantane and 10 g of anhydrous aluminum bromide were placed therein, and then the inside of the flask was cooled to 0° C. Thereto was added 190 g of 1,3-dibromobenzene that was cooled to 5° C. in advance, and the resulting material was agitated and reacted at an inside temperature of 0 to 10° C. for 7 hours. The reaction was carried out while the hydrogen bromide gas that was generated during the reaction was absorbed into an aqueous alkaline solution for the removal of its toxicity. After the completion of the reaction, 130 g of 4% by weight hydrochloric acid was slowly dropped and then the solution was stirred until the orange color of the reaction solution faded away. The agitation was stopped and the resulting solution was allowed to stand and then separated by funnel. The resulting organic phase was washed with water three times. 190 grams of toluene was added to the organic phase after the washing, which was then warmed to remove water under reflux. Then, the organic solution was cooled and the crystal deposited was collected by filtration. The resulting crystal was subjected to washing with toluene, methanol and water, followed by drying under reduced pressure to obtain 44 g of 1,3-bis(3,5-dibromophenyl)adamantane.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07084287B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-056f03b2844a43409ccd9457a545328f
Quellennotizuspto-grants-2006_08