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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1357879생성일: 2026년 10월 26일

Dimethyl Sulfoxide → 9-(1-Propen-1-yl)-9H-carbazole

https://huagongshe.com/reaction/1357879

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfoxideHCID 679—
반응물9-AllylcarbazoleHCID 3090393—
반응물Potassium tert-butoxideHCID 23665647—
용매WaterHCID 962—
생성물9-(1-Propen-1-yl)-9H-carbazoleHCID 375335363%

반응 단계

Into a 100 mL round bottom flask fitted with a magnetic stirrer, reflux condenser and nitrogen inlet were placed 2.07 g (0.01 mole) of 9-allyl carbazole, 1.12 g (0.01 mole) of potassium t-butoxide and 10 mL of DMSO. The reaction mixture was stirred for 20 minutes at room temperature and then was heated to 120° C. and kept at that temperature for two hours. TLC on silica gel was used to monitor the reaction. After cooling to room temperature, the reaction mixture was poured into 20 mL of distilled water and extracted with ethyl ether. The organic layer was washed with distilled water to remove DMSO, then anhydrous sodium sulfate was added and the mixture stirred for an hour. Thereafter, the sodium sulfate was removed by filtration and a rotary evaporator was used to remove the solvent. 9-(1-Propenyl)carbazole was isolated in 63% yield (1.3 g) as a pale yellow viscous liquid. 1H NMR (300 MHz, CDCl3) showed that the product was consisted of approximately a 1:2 ratio of cis and trans 9-(1-propenyl)carbazole isomers.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06593388B2
출처 데이터셋uspto-grants-2003_07
ORD IDord-2ee24238f0154a6bb3a39bb0ba86e6e9
출처 메모uspto-grants-2003_07