Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 245803Erstellt: 23. Oktober 2026

Sodium hydride → 6-bromo-1-(2-trimethylsilanyl-ethoxymethyl)-1H-indazole

https://huagongshe.com/de/reaction/245803

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
Edukt2-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 2724271—
Edukt6-Bromo-1H-indazoleHCID 17842471—
LösungsmittelDimethylformamideHCID 6228—
Produkt6-bromo-1-(2-trimethylsilanyl-ethoxymethyl)-1H-indazoleHCID 6736195769%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

In a round-bottomed flask 6-bromo-1H-indazole (0.70 g, 3.55 mmol) was dissolved in DMF (7.5 ml). The reaction mixture was cooled to 0° C. and sodium hydride (60% dispersion in mineral oil, 172 mg, 4.3 mmol) was added). The reaction mixture was warmed to room temperature and stirred for 30 min then cooled back to 0° C. and SEM-Cl (0.76 ml, 4.28 mmol) was slowly added. After the addition was complete, the ice bath was removed and the reaction mixture was warmed to room temperature. After 1.5 h the reaction was quenched with water and extracted with diethyl ether (2×). The combined organic layers were washed twice with water and once with brine then dried over sodium sulfate, filtered and concentrated. The residue was chromatographed over silica gel with EtOAc/Hexanes (gradient 0-10% EtOAc) to give 802 mg (69%) of 6-bromo-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-31e08321afa54c9e94d4e7503a8b71a5
Quellennotizuspto-grants-2014_02