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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 12219Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/12219

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktMethyl iodideHCID 6328—
EduktSodium bis(trimethylsilyl)amideHCID 2724254—
Edukttert-Butyl 3-(cyanomethyl)-1H-indole-1-carboxylateHCID 15378323—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
Produkt2-(1-Tert-butoxycarbonylindol-3-yl)propionitrileHCID 2522306979,4%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07727985B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-1a045f84366a4f88ac017f6c5af9c4fc
Quellennotizuspto-grants-2010_06