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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 488538Erstellt: 24. Oktober 2026

Indole → 1-Benzylindole

https://huagongshe.com/de/reaction/488538

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIndoleHCID 798—
EduktEthyl AcetateHCID 8857—
EduktDabcoHCID 9237—
EduktDimethylacetamideHCID 31374—
KatalysatorTetrabutylammonium ChlorideHCID 70681—
LösungsmittelWaterHCID 962—
Produkt1-BenzylindoleHCID 9691380%

Reaktionsbedingungen

Temperatur135 °C

Reaktionsschritte

To a mixture of indole (234 mg, 2.0 mmol), DBC (726 mg, 3.0 mmol), DABCO (67.2 mg, 0.6 mmol) and TBAC (556 mg, 2.0 mmol) is added DMA (4 mL). The resulting solution is heated at 135° C. for 2 h. The reaction mixture is cooled to RT and diluted with EtOAc (50 mL) and H2O (50 mL). The two layers are separated and the aqueous layer is back extracted with EtOAc (50 mL). The combined organic layers are washed with brine and dried over anhydrous Na2SO4. The mixture is filtered and concentrated under vacuum. The crude residue is purified with Biotage Flash Chromatography unit on 40 s cartridge eluting with hexane:CH2Cl2=19:1 solvent mixture to afford 1-benzylindole (about 331.2 mg, 80%) as a white solid: mp 43° C.; 1H NMR (CDCl3) δ7.38 (m, 9H), 6.73 (d, 1H), 5.48 (s, 2H); 13C NMR (CDCl3) δ137.5, 136.3, 128.7, 128.2, 127.6, 126.7, 121.6, 120.9, 119.5, 109.7, 101.6, 50.0; MS m/z 207.1043 [M+1]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06972336B2
Quelldatensatzuspto-grants-2005_12
ORD IDord-da8e818df7b34bd69a9e779ff363a5cb
Quellennotizuspto-grants-2005_12