Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 902553Erstellt: 25. Oktober 2026

4-Heptanone → 4-(7-bromo-2-methyl-2H-indazol-3-yl)-heptan-4-ol

https://huagongshe.com/reaction/902553

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-HeptanoneHCID 31246—
EduktSodium BicarbonateHCID 516892—
EduktLithium diisopropylamideHCID 2724682—
Edukt7-bromo-2-methyl-2H-indazoleHCID 21094580—
EduktTetrahydrofuran heptane ethylbenzolHCID 22742125—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-(7-bromo-2-methyl-2H-indazol-3-yl)-heptan-4-olHCID 2109458978%

Reaktionsbedingungen

Temperatur2.5 °C

Reaktionsschritte

To a solution of 7-bromo-2-methyl-2H-indazole (1.5 g, 7.1 mmol) in 18 mL of THF at −78° C. was added a 2 M solution of lithium diisopropylamide in heptane/ethylbenzene/THF (5.3 mL, 11 mmol). The solution was stirred at 0-5° C. for 10 m, then rechilled to −78° C. To it was added 4-heptanone (1.49 mL, 10.6 mmol), and the solution was stirred overnight, allowing to slowly warm to room temperature. A saturated aqueous NaHCO3 solution (40 mL) was added, and the mixture was extracted with three 30 mL portions of ethyl acetate. The combined organic layers were dried over Na2SO4, filtered, and concentrated to a brown solid. Column chromatography (0→20% EtOAc/hexanes) afforded 4-(7-bromo-2-methyl-2H-indazol-3-yl)-heptan-4-ol (42; 1.80 g; 78%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07365211B2
Quelldatensatzuspto-grants-2008_04
ORD IDord-ef09b8f2e6f547d09b8fcedd28f5bf1f
Quellennotizuspto-grants-2008_04