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HRID 17622作成日:2026年10月24日

Methyl iodide → tert-Butyl methyl-(3-tri-n-butylstannylcyclopent-2-enyl)carbamate

https://huagongshe.com/ja/reaction/17622

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物Sodium hydrideHCID 24758—
反応物Ammonium ChlorideHCID 25517—
反応物Tert-butyl (3-tri-n-butylstannylcyclopent-2-enyl)carbamateHCID 15630117—
溶媒DimethylformamideHCID 6228—
生成物tert-Butyl methyl-(3-tri-n-butylstannylcyclopent-2-enyl)carbamateHCID 6858496996.1%

反応手順

Tert-butyl (3-tri-n-butylstannylcyclopent-2-enyl)carbamate (2.0 g, 4.24 mmol) was dissolved in N,N-dimethylformamide (40 ml), and at 0° C., methyl iodide (527 μl, 8.47 mmol) and then sodium hydride (55%, w/w), (277 mg, 6.35 mmol) were added. With gradually warming from 0° C. up to room temperature, this was stirred for 24 hours. At 0° C., aqueous saturated ammonium chloride solution was added to the solution, followed by stirring at the same temperature for 30 minutes. The solution was extracted three times with ethyl acetate. The organic layers were combined, washed with saturated brine, and dried over anhydrous sodium sulfate. The insoluble matter was separated by filtration, the solvent was evaporated away, and the resulting residue was purified by middle-pressure liquid chromatography (eluent, n-hexane:ethyl acetate=99:1, v/v) to obtain a colorless oil (1.982 g, 96%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737166B2
出典データセットuspto-grants-2010_06
ORD IDord-6e43b11caf5d4fa8a96eac542119e500
出典メモuspto-grants-2010_06