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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 259352생성일: 2026년 10월 24일

Acridone → 9-(p-Vinylphenyl)acridine

https://huagongshe.com/ko/reaction/259352

반응식

참여 물질

역할이름HCID투입량
반응물AcridoneHCID 2015—
반응물Phosphorus oxide (P4O10)HCID 14812—
반응물4-BromostyreneHCID 16263—
반응물MagnesiumHCID 5462224—
용매BenzeneHCID 241—
용매TetrahydrofuranHCID 8028—
생성물9-(p-Vinylphenyl)acridineHCID 2276087042.1%

반응 단계

Into a four-neck flask equipped with a stirrer, a nitrogen gas inlet tube, a reflux condenser with a calcium chloride tube and a dropping funnel were charged 4.9 g of magnesium cut powder and 50 ml of tetrahydrofuran. 36.6 Grams of p-bromostyrene diluted with tetrahydrofuran to about 4 times the weight was added dropwise under gentle reflux in a dry nitrogen gas stream. After the magnesium had disappeared, a solution consisting of 37.0 g of acridone and 600 ml of tetrahydrofuran was added dropwise over a period of two hours with stirring. After refluxing for further 5 hours, the reaction mixture was allowed to cool and then poured onto hydrochloric acid-ice to effect hydrolysis. The organic layer was extracted with ether and the extract was dried over anhydrous sodium sulfate. The solvent was then distilled off to obtain a yellow semi-solid. Almost the same weight (60 g) of phosphorus pentoxide was added to 500 ml of a solution of the semi-solid in benzene. The mixture was stirred at room temperature for 5 hours and then allowed to stand overnight. The supernatant liquid separated by decantation was washed with water, dried, and then concentrated to dryness. The residue was purified by silica gel chromatography to obtain 22.5 g of 9-(p-vinylphenyl)acridine. Yield 42.1%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04037036
출처 데이터셋uspto-grants-1977_07
ORD IDord-82ce3c7a56db4801884c65dfdfdef387
출처 메모uspto-grants-1977_07