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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 36382생성일: 2026년 10월 24일

Acetonitrile → 9-Allylcarbazole

https://huagongshe.com/ko/reaction/36382

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물CarbazoleHCID 6854—
반응물Allyl bromideHCID 7841—
반응물Potassium CarbonateHCID 11430—
용매DichloromethaneHCID 6344—
생성물9-AllylcarbazoleHCID 3090393—

반응 단계

Into a 500-mL, three-necked, round-bottomed flask, equipped with a magnetic stirrer, a thermometer, and a condenser connected to a nitrogen bubbler, were placed carbazole (8.4 g, 50 mmole), allyl bromide (10 mL, 115 mmole), powdered anhydrous potassium carbonate (41 g, 300 mmole), and anhydrous acetonitrile (300 mL). The resultant mixture was stirred and heated under reflux with a heating mantle for 18 hours. Dichloromethane (300 mL) was then added, and the mixture was filtered through a pad of Celite. The clear filtrate was evaporated, and the residue was recrystallized from methanol to yield the desired product as amber-colored crystals. The product had melting point 56°-57° C., and sublimation (100° C./0.1 mm Hg) yielded white crystals (8.65 g, 83%), melting point 57°-58° C. The proton NMR spectrum in carbon tetrachloride was

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05414069
출처 데이터셋uspto-grants-1995_05
ORD IDord-2db01ce7b32a46519cdefc6ef82ad7c5
출처 메모uspto-grants-1995_05