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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 61754생성일: 2026년 10월 26일

1-Propanol → 6,6-Dimethyl-11-oxo-8-vinyl-6,11-dihydro-5H-benzo[b]carbazole-3-carbonitrile

https://huagongshe.com/reaction/61754

반응식

참여 물질

역할이름HCID투입량
반응물1-PropanolHCID 1031—
반응물TriethylamineHCID 8471—
반응물Potassium vinyltrifluoroborateHCID 23679353—
반응물Trifluoro-methanesulfonic acid 3-cyano-6,6-dimethyl-11-oxo-6,11-dihydro-5H-benzo[b]carbazol-8-yl esterHCID 86663817—
용매WaterHCID 962—
생성물6,6-Dimethyl-11-oxo-8-vinyl-6,11-dihydro-5H-benzo[b]carbazole-3-carbonitrileHCID 6683405480%

반응 조건

온도60 °C

반응 단계

Under nitrogen atmosphere, trifluoro-methanesulfonic acid 3-cyano-6,6-dimethyl-11-oxo-6,11-dihydro-5H-benzo[b]carbazol-8-yl ester (Compound B1, 1.00 g, 2.302 mmol) was added with n-propanol (20 mL), potassium vinyltrifluoroborate (854 mg, 3.0 eq.), dichloro-((bis-diphenylphosphino)ferrocenyl)palladium (217 mg, 0.1 eq.) and triethylamine (1.11 ml, 3.0 eq.) in order and the resultant was stirred at 60° C. for 4 hr. Upon the completion of the reaction, water was added to the reaction solution. The resulting precipitates were filtered and washed with distilled water, and the residues were dried to obtain the title compound (666 mg, 80%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09440922B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-27637dfe19f8455bb26f5e4928000c58
출처 메모uspto-grants-2016_09