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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1467430Erstellt: 23. Oktober 2026

Triethylsilane → 1-benzyl-2-(triethylsilyl)-1H-indole

https://huagongshe.com/de/reaction/1467430

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylsilaneHCID 12052—
Edukt1-BenzylindoleHCID 96913—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-benzyl-2-(triethylsilyl)-1H-indoleHCID 9009596731,1%

Reaktionsschritte

The reaction was conducted according to the General Procedure by heating 1-benzylindole (62 mg, 0.5 mmol, 1 equiv.), KOt-Bu (11 mg, 0.1 mmol, 0.2 equiv) and Et3SiH (239 microliters, 1.5 mmol, 3 equiv.) in 1 mL of tetrahydrofuran for 48 hours at 23° C. After aqueous work up, the crude reaction mixture was purified by chromatography on silica using hexanes (isochratic) to obtain 50 mg (31%) of the title compound as a colourless oily solid. 1H NMR (500 MHz, THF-d8) δ 7.56 (ddd, J=7.7, 1.3, 0.7 Hz, 1H), 7.25-7.07 (m, 4H), 7.02 (ddd, J=8.2, 6.9, 1.3 Hz, 1H), 6.98 (ddd, J=7.9, 6.9, 1.1 Hz, 1H), 6.92-6.86 (m, 2H), 6.80 (d, J=0.9 Hz, 1H), 5.52 (s, 2H), 1.06-0.88 (m, 9H), 0.85-0.69 (m, 6H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09000167B2
Quelldatensatzuspto-grants-2015_04
ORD IDord-0dd02e7cdf2b4b629a3dce84c265c422
Quellennotizuspto-grants-2015_04