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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 54026생성일: 2026년 10월 24일

Hydrochloric Acid → Naphthylboric acid

https://huagongshe.com/ko/reaction/54026

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Phosphoric AcidHCID 1004—
반응물1-BromonaphthaleneHCID 7001—
반응물HexaneHCID 8058—
반응물Trimethyl borateHCID 8470—
반응물ButyllithiumHCID 178418339—
촉매PhenothiazineHCID 7108—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물Naphthylboric acidHCID 1386291446.5%

반응 조건

온도-78 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05621129
출처 데이터셋uspto-grants-1997_04
ORD IDord-ef63277f97274c24a27ecc2710e12653
출처 메모uspto-grants-1997_04