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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 68514생성일: 2026년 10월 24일

Hydrochloric Acid → 2,10-Di(2-naphthyl)anthracene

https://huagongshe.com/ko/reaction/68514

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물2-BromonaphthaleneHCID 11372—
반응물2-(2-Naphthyl)-10-anthroneHCID 58194450—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물2,10-Di(2-naphthyl)anthraceneHCID 5819427632%

반응 조건

온도-78 °C

반응 단계

Under an argon atmosphere, a solution of 4.81 g of 2-bromonaphthalene in 30 mL of THF was cooled to −78° C. Subsequently, 25 mL of a 1.6-M solution of n-butyllithium in hexane were dropped to the solution, and then the mixture was stirred at −78° C. for 1 hour. A solution of 6.76 g of 2-(2-naphthyl)-10-anthrone in 20 mL of THF was added to the mixture, and then the resultant reaction solution was stirred for 5 hours at 50° C. under heat. After the reaction solution had been cooled to room temperature, 100 mL of 10% hydrochloric acid were added to the solution. After the water layer had been removed, the organic layer was washed with water and a saturated salt solution. Then, the organic layer was dried with magnesium sulfate. The solvent was removed by distillation under reduced pressure, and then the residue was purified by silica gel column chromatography. Thus, 2.90 g of 2,10-di(2-naphthyl)anthracene were obtained (in 32% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822041B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-ad9f616da4e343db967793d8c8e55f3d
출처 메모uspto-grants-2014_09