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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 343102Erstellt: 24. Oktober 2026

Diisobutylaluminum hydride → (1-methyl-1H-indazol-3-yl)methanol

https://huagongshe.com/de/reaction/343102

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisobutylaluminum hydrideHCID 14487—
EduktMethyl 1-methyl-1H-indazole-3-carboxylateHCID 13900574—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelHexaneHCID 8058—
Produkt(1-methyl-1H-indazol-3-yl)methanolHCID 716454690,8%

Reaktionsschritte

To a stirring solution of 440 mg (2.31 mmol) of 1-Methyl-1H-indazole-3-carboxylic acid methyl ester (Fludzinski, P. et. al. J. Med. Chem. 1987, 30, 1535) in 10 mL dichloromethane at -78° C. is added dropwise over 5 min a solution of 5.8 mL (5.8 mmol, 2.5 equiv) of a 1.0M solution of DIBAL-H in hexane. The resulting solution is allowed to slowly warm to RT over a 3 h period then quenched by careful addition of 5 mL of H2O. The reaction mixture is poured into 100 mL of EtOAc and extracted with 1N HCl (1×100 mL), dried (MgSO4), and the solvent removed in vacuo. Purification of the crude material by silica gel flash column chromatography using hexane/EtOAc 1/1 as eluent afforded 340 mg of the title compound as a pale yellow oil: 1H NMR (CDCl3, 300 MHz) δ7.80 (d, 1H), 7.42-7.12 (m, 3H), 5.02 (d, 2H), 4.00 (s, 3H), 2.27 (m, 1H); Rf =0.25 in hexane/EtOAc 1/1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05859007
Quelldatensatzuspto-grants-1999_01
ORD IDord-ac953208cf3144fca98e034a61833c8f
Quellennotizuspto-grants-1999_01