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HRID 7221作成日:2026年10月23日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrogen BromideHCID 260—
反応物1,3-DibromobenzeneHCID 7927—
反応物BromhydrolHCID 166749—
反応物1,3-DibromoadamantaneHCID 265790—
生成物1,3-Bis(3,5-dibromophenyl)adamantaneHCID 22020297194.3%

反応条件

温度0 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07084287B2
出典データセットuspto-grants-2006_08
ORD IDord-056f03b2844a43409ccd9457a545328f
出典メモuspto-grants-2006_08