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HRID 54026作成日:2026年10月25日

Hydrochloric Acid → Naphthylboric acid

https://huagongshe.com/reaction/54026

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Phosphoric AcidHCID 1004—
反応物1-BromonaphthaleneHCID 7001—
反応物HexaneHCID 8058—
反応物Trimethyl borateHCID 8470—
反応物ButyllithiumHCID 178418339—
触媒PhenothiazineHCID 7108—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物Naphthylboric acidHCID 1386291446.5%

反応条件

温度-78 °C

反応手順

To a solution of 1-bromonaphthalene (10 g, 48 mmol) in THF (100 ml), a 1.65 M solution of n-butyl lithium in n-hexane (58 ml, 96 mmol of n-butyl lithium) and stirred at -78° C. for one hour. Then, trimethoxyborane (10 g, 96 mmol) was added, and the mixture was stirred at -78° C. for 30 minutes, and then at room temperature for one hour. To the mixture, phenothiazine (132 mg) and then a mixture of conc. hydrochloric acid (20 ml), phosphoric acid (30 ml) and water (220 ml) were gradually added. After heating the mixture to room temperature and stirring it for 20 hours, the organic layer was separated. The aqueous solution was washed with diethyl ether. The combined organic layer was washed with a 10% aqueous solution of sodium chloride. To the ice-cooled organic layer, a 5% aqueous solution of sodium hydroxide was added and stirred. Then, the mixture was phase separated, and the aqueous layer was saturated with sodium chloride, acidified with phosphoric acid, and extracted with diethyl ether. The diethyl ether layer was dried over anhydrous magnesium sulfate. The solvent was evaporated off, and the obtained solid residue was recrystallized from ethyl acetate/n-hexane to obtain naphthylboric acid (4.20 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05621129
出典データセットuspto-grants-1997_04
ORD IDord-ef63277f97274c24a27ecc2710e12653
出典メモuspto-grants-1997_04