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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 246338Generated: October 30, 2026

Diisobutylaluminum hydride → (3-iodo-1-methyl-1H-indazol-5-yl)methanol

https://huagongshe.com/reaction/246338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantMethyl 3-iodo-1-methyl-1H-indazole-5-carboxylateHCID 71279594—
SolventDichloromethaneHCID 6344—
Product(3-iodo-1-methyl-1H-indazol-5-yl)methanolHCID 7128009293.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 3-iodo-1-methyl-1H-indazole-5-carboxylic acid methyl ester (0.95 g, 3.01 mmol) in CH2Cl2 (30 mL) at 0° C. was slowly added DIBAL-H (1.18 mL, 6.61 mmol). The reaction mixture was stirred at 0° C. for 1.5 h. Carefully quenched with MeOH (1 mL) then diluted with CH2Cl2 (20 mL) and added saturated aqueous Na+K+ tartrate (30 mL). The biphasic mixture was stirred vigorously at room temp for 1 h. The layers were separated and the aqueous phase was extracted with CH2Cl2. The combined organics were washed with water then dried over MgSO4 and concentrated to afford 810 mg of (3-iodo-1-methyl-1H-indazol-5-yl)methanol as a yellow waxy solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658646B2
Source datasetuspto-grants-2014_02
ORD IDord-2bc6f15d51aa4840af5cc95f4a7e8df8
Source noteuspto-grants-2014_02