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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1950생성일: 2026년 10월 23일

Methanol → 5-{N-[4-(4-methylstyryl)phenyl]-N-phenylamino}acenaphthene

https://huagongshe.com/ko/reaction/1950

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물WaterHCID 962—
반응물5-[N-(4-formylphenyl)-N-phenylamino]acenaphtheneHCID 19688917—
반응물Potassium tert-butoxideHCID 23665647—
용매DimethylformamideHCID 6228—
생성물5-{N-[4-(4-methylstyryl)phenyl]-N-phenylamino}acenaphtheneHCID 6764361285%

반응 단계

20.96 g (0.06 mol) of 5-[N-(4-formylphenyl)-N-phenylamino]acenaphthene prepared in Preparation Example 1 and 17.44 g (0.072 mol) of diethyl 4-methylbenzyl phosphonate were dissolved in 300 ml of N,N-dimethylformamide, and 10.1 g (0.09 mol) of potassium-tert-butoxide was added thereto at room temperature for 20 minutes. After the addition, the resultant mixture was further stirred for 2 hours. The reaction was determined to be finished when disappearance of the formyl compound was identified. The reaction product was poured into 1500 ml of methanol at a temperature of 5° C. or lower, and 150 ml of water was further dropwise added thereto to precipitate a crystal, which was then filtrated, washed with methanol and dried to obtain 22.18 g (yield: 84.5%) of a crude crystal. 21.0 g of the crude crystal thus obtained was purified by column chromatography (carrier: silica gel, eluent: toluene/hexane=1/4) to obtain 17.85 g of (purification yield: 85.0%, melting point: 148.0°-149.0° C.) of 5-{N-[4-(4-methylstyryl)phenyl]-N-phenylamino}acenaphthene (Compound No. 4).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05728500
출처 데이터셋uspto-grants-1998_03
ORD IDord-b58f8f3df4214a82901f48cbd358ba6b
출처 메모uspto-grants-1998_03