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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 245804Erstellt: 23. Oktober 2026

Toluene → 6-cyclopropyl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-indazole

https://huagongshe.com/de/reaction/245804

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTolueneHCID 1140—
EduktPotassium Phosphate, TribasicHCID 62657—
EduktCyclopropylboronic acidHCID 2760897—
Edukt6-bromo-1-(2-trimethylsilanyl-ethoxymethyl)-1H-indazoleHCID 67361957—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelWaterHCID 962—
Produkt6-cyclopropyl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-indazoleHCID 7128033895,2%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A round-bottomed flask was charged with 6-bromo-1-(2-trimethylsilanyl-ethoxymethyl)-1H-indazole (0.80 g, 2.44 mmol), cyclopropylboronic acid (377 mg, 4.39 mmol), palladium(II) acetate (28 mg, 0.125 mmol), potassium phosphate tribasic (1.04 g, 4.88 mmol), toluene (9 ml) and water (0.9 ml). The reaction mixture was stirred at 100° C. in an oil bath overnight then cooled to room temperature, quenched with water and extracted with EtOAc (2×). The combined organic layers were washed with water and brine then dried over sodium sulfate, filtered and concentrated. The residue was chromatographed over silica gel with EtOAc/Hexanes (gradient 0-5% EtOAc) to afford 670 mg (90%) of 6-cyclopropyl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-indazole as a light yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08658646B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-c18be89c1d6c4caba5d0593ea777c4b6
Quellennotizuspto-grants-2014_02