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HRID 36382作成日:2026年10月25日

Acetonitrile → 9-Allylcarbazole

https://huagongshe.com/reaction/36382

反応式

関与物質

役割名称HCID仕込み量
反応物AcetonitrileHCID 6342—
反応物CarbazoleHCID 6854—
反応物Allyl bromideHCID 7841—
反応物Potassium CarbonateHCID 11430—
溶媒DichloromethaneHCID 6344—
生成物9-AllylcarbazoleHCID 3090393—

反応手順

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

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05414069
出典データセットuspto-grants-1995_05
ORD IDord-2db01ce7b32a46519cdefc6ef82ad7c5
出典メモuspto-grants-1995_05