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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12219생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/12219

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참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Methyl iodideHCID 6328—
반응물Sodium bis(trimethylsilyl)amideHCID 2724254—
반응물tert-Butyl 3-(cyanomethyl)-1H-indole-1-carboxylateHCID 15378323—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물2-(1-Tert-butoxycarbonylindol-3-yl)propionitrileHCID 2522306979.4%

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온도0 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07727985B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-1a045f84366a4f88ac017f6c5af9c4fc
출처 메모uspto-grants-2010_06