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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1983459Generated: October 26, 2026

Ethyl Acetate → 2-(3-(3-Fluorophenyl)-1H-5-indazolyl]acetonitrile

https://huagongshe.com/reaction/1983459

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium CyanideHCID 8929—
Reactant1h-Indazole-1-carboxylic acid,5-(chloromethyl)-3-(3-fluorophenyl)-,1,1-dimethylethyl esterHCID 22260616—
SolventDimethyl SulfoxideHCID 679—
Product2-(3-(3-Fluorophenyl)-1H-5-indazolyl]acetonitrileHCID 222606228.9%

Reaction Steps

To a solution of 1.0 g of tert-butyl 5-(chloromethyl)-3-(3-fluorophenyl)-1H-1-indazolecarboxylate in 5 ml dimethyl sulfoxide was added 204 mg of sodium cyanide, and the mixture was stirred at room temperature for 50 minutes. To the reaction mixture was added 50 ml of ethyl acetate, and after washing with water, the aqueous layer was re-extracted with diethyl ether. The collected organic layer was sequentially washed with water (×2) and brine, dried over anhydrous magnesium sulfate and the solvent was evaporated. The crude product was purified and separated by silica gel column chromatography (ethyl acetate:toluene=1:9), and suspended in diethyl ether-diisopropyl ether, to give 62 mg of the title compound as yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07541376B2
Source datasetuspto-grants-2009_06
ORD IDord-f8fc6e0e81fd48f4a5f0eeec40e7fc8e
Source noteuspto-grants-2009_06