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HRID 984491作成日:2026年10月25日

Carbon Dioxide → 5-iodo-1-methyl-1H-indole

https://huagongshe.com/reaction/984491

反応式

関与物質

役割名称HCID仕込み量
反応物Carbon DioxideHCID 280—
反応物Methyl iodideHCID 6328—
反応物Sodium hydrideHCID 24758—
反応物5-Iodo-1H-indoleHCID 2782313—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物5-iodo-1-methyl-1H-indoleHCID 11322835—

反応手順

To a solution of 5-iodoindole (75 g, 0.31 mol) in dry THF (750 mL), at −78° C. was added sodium hydride (60% in mineral oil, 14.85 g, 0.37 mol) in one portion. The suspension was stirred at −78° C. for 1 hour after which iodomethane (28.8 mL, 0.46 mol) was added. The reaction mixture was stirred overnight with a slow elevation of temperature to room temperature (no more dry ice was added). Ether (600 mL) and hexane (1.2 L) were added and the mixture was washed with brine (1.6 L) and water (1.5 L), dried over Na2SO4 and filtered. The solution was concentrated and the residual brown solid was recrystallized from hexane to give the title compound (66 g). The impure fraction from the mother liquor was flash chromatographed (8% EtOAc in hexane) to give an additional quantity of desired product (12.5 g, combined yield of 99%). MS (DCI/NH3) m/e 258 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06867203B2
出典データセットuspto-grants-2005_03
ORD IDord-5ed9a02dfa824f8b99de2715a2e404ae
出典メモuspto-grants-2005_03