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HRID 12219作成日:2026年10月26日

Water → 2-(1-Tert-butoxycarbonylindol-3-yl)propionitrile

https://huagongshe.com/reaction/12219

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Methyl iodideHCID 6328—
反応物Sodium bis(trimethylsilyl)amideHCID 2724254—
反応物tert-Butyl 3-(cyanomethyl)-1H-indole-1-carboxylateHCID 15378323—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物2-(1-Tert-butoxycarbonylindol-3-yl)propionitrileHCID 2522306979.4%

反応条件

温度0 °C

反応手順

A stirred solution of 3-cyanomethyl-indole-1-carboxylic acid tert-butyl ester (2.15 g, 8.39 mmol) in THF (40 ml) was cooled to −78° C. under an argon atmosphere. Sodium bis(trimethylsilyl)amide (1 M in THF, 10 ml, 10 mmol) was added thereto and the cold solution was stirred for 30 minutes. Iodomethane (627 uL, 10 mmol) was added thereto and the reaction mixture was stirred 1.5 hr while gradually warming to 0° C. H2O (100 ml) was added thereto and the solution was brought to RT and diluted with EtOAc (250 ml). The aqueous layer was removed and extracted with EtOAc (250 ml). The combined organic layers were washed with aqueous HCl (1N, 3×50 ml), followed by brine, then dried over MgSO4, filtered, and concentrated to an orange oil. Purification via column chromatography (hexanes:ethyl acetate) gave 3-(cyano-methyl-methyl)-indole-1-carboxylic acid tert-butyl ester (1.8 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07727985B2
出典データセットuspto-grants-2010_06
ORD IDord-1a045f84366a4f88ac017f6c5af9c4fc
出典メモuspto-grants-2010_06