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HRID 1045282作成日:2026年10月27日

Hydrochloric Acid → 9-Anthraceneboronic Acid

https://huagongshe.com/reaction/1045282

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Trimethyl borateHCID 8470—
反応物9-BromoanthraceneHCID 74062—
反応物HCID 178418244HCID 178418244—
溶媒TolueneHCID 1140—
溶媒TetrahydrofuranHCID 8028—
生成物9-Anthraceneboronic AcidHCID 1551021373%

反応条件

温度-40 °C

反応手順

9-Bromoanthracene 38.6 g was dissolved in dehydrated toluene 80 ml and dehydrated THF (tetrahydrofuran) 160 ml, and the solution was cooled to −40° C. A 1.58M n-butyllithium hexane solution 106 ml was dropwise added thereto and stirred at −40° C. for 30 minutes, the temperature was elevated up to −10° C. The solution was cooled again down to −70° C., and a dehydrated THF solution of trimethyl borate 50.0 ml was gradually dropwise added thereto. The solution was stirred at −70° C. for 2 hours and then slowly heated up to room temperature. After left standing for a night, a 10% hydrochloric acid aqueous solution 100 ml was added thereto and stirred, and then it was extracted twice with toluene. The organic layer was washed with saturated brine and dried on anhydrous sodium sulfate. The solvent was distilled off, and the residue was crystallized from toluene/hexane, filtered and dried, whereby targeted 9-anthraceneboronic acid 24.4 g was obtained in the form of pale brown crystal (yield: 73%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08568902B2
出典データセットuspto-grants-2013_10
ORD IDord-25684892488041d6bc926e998e4c2101
出典メモuspto-grants-2013_10