Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1805899Erstellt: 25. Oktober 2026

Ethyl 2-hydroxyisobutyrate → Bindarit

https://huagongshe.com/reaction/1805899

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl 2-hydroxyisobutyrateHCID 6653—
EduktSodium HydroxideHCID 14798—
EduktSodium hydrideHCID 24758—
Edukt1-Benzyl-3-(chloromethyl)-1H-indazoleHCID 53260648—
LösungsmittelTolueneHCID 1140—
LösungsmittelDimethylformamideHCID 6228—
ProduktBindaritHCID 71354—

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

Ethyl-2-hydroxyisobutyrate (18.5 g, 140 mmol, 1.2 eq.), toluene (100 mL) and DMF (20 mL) were placed in a three-necked flask fitted with a mechanical stirrer and a reflux condenser under an inert atmosphere. A dispersion of 60% NaH (5.6 g, 140 mmol, 1.2 eq.) was added to the mixture in portions over a period of approximately 1.5 hours. A solution of 1-benzyl-3-chloromethyl-1H-indazole (30 g, 117 mmol, 1 eq.) in toluene (90 mL) and DMF (60 mL) was then added dropwise. The reaction mixture was heated to approximately 90° C. and kept at that temperature until the reaction was complete (checked by TLC, approximately 10 hours). After cooling to room temperature the mixture was washed with acidified water and water. The organic phase was concentrated under reduced pressure and the oily residue obtained was treated with 10 M NaOH (36 mL) at reflux temperature for at least 3 hours. The product, which was precipitated out by the addition of concentrated HCl, was filtered and dried. Yield: 32.3 g of white solid (85%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08354544B2
Quelldatensatzuspto-grants-2013_01
ORD IDord-2c18832d61fa488fbdcc6bd55ad55ec3
Quellennotizuspto-grants-2013_01