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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 877291생성일: 2026년 10월 24일

Ethanol → 4-(7-Phenylbenz[a]anthracen-4-yl)-7-phenylbenz[a]anthracene

https://huagongshe.com/ko/reaction/877291

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물Phenylboronic AcidHCID 66827—
반응물N-bromobutanimideHCID 67184—
반응물4-(Benz[a]anthracen-4-yl)benz[a]anthraceneHCID 59412552—
용매DimethylformamideHCID 6228—
생성물4-(7-Phenylbenz[a]anthracen-4-yl)-7-phenylbenz[a]anthraceneHCID 59412710—

반응 단계

19.6 g (110 mmol) of N-bromosuccinimide are added in one portion at 100° C. with vigorous stirring to a suspension of 22.7 g (50 mmol) of 4-(benz[a]anthracen-4-yl)benz[a]anthracene in 1000 ml of DMF. The suspension is kept at 100° C. for a further 30 min. and cooled, and 1000 ml of ethanol are then added. The precipitated solid is filtered off with suction, washed three times with 100 ml of ethanol each time and dried in vacuo. The resultant solid is reacted analogously to Example 7 with 15.9 g (130 mmol) of benzeneboronic acid, Recrystallisation five times from DMF (about 6 ml/g); sublimation (p=5×10−5 mbar, T=360° C.). Yield: 21.8 g (36 mmol), 72.0%, purity 99.9% (HPLC), Tg=181.4° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08986852B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-52646a4582bf43ba9c9fb5c133992734
출처 메모uspto-grants-2015_03