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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602403Generated: October 30, 2026

Sodium hydride → 2-Bromo-4-(6,6-dimethyl-4-oxo-3-difluoromethyl-4,5,6,7-tetrahydroindazol-1-yl)-benzonitrile

https://huagongshe.com/reaction/602403

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-Bromo-4-fluorobenzonitrileHCID 118939—
Reactant3-Difluoromethyl-6,6-dimethyl-1,5,6,7-tetrahydro-indazol-4-oneHCID 44190349—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventAmmonium ChlorideHCID 25517—
Product2-Bromo-4-(6,6-dimethyl-4-oxo-3-difluoromethyl-4,5,6,7-tetrahydroindazol-1-yl)-benzonitrileHCID 1185468649.2%

Reaction Steps

NaH (350 mg) was added to a solution of 3-difluoromethyl-6,6-dimethyl-1,5,6,7-tetrahydro-indazol-4-one (3.12 g) in DMSO (75 mL) at room temperature. After 20 minutes of stirring, 2-bromo-4-fluorobenzonitrile (4.67 g) was added and stirred at 45° C. overnight. The reaction was diluted with saturated aqueous NH4Cl (100 mL), H2O (100 mL). The mixture was extracted with ethyl acetate (4×150 mL), dried over Na2SO4, filtered, concentrated, purified by column chromatography eluting with a 1:2 mixture of ethyl acetate/hexanes. The concentrate of desired fractions was made into a slurry in ether, stirred for 2 h, filtered, washed by hexane to give pure solid 2-bromo-4-(6,6-dimethyl-4-oxo-3-difluoromethyl-4,5,6,7-tetrahydro-indazol-1-yl)-benzonitrile (2.82 g, 49.2%). LCMS m/z: (M+H)=395.65, (MW: 394).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906529B2
Source datasetuspto-grants-2011_03
ORD IDord-019f5e49b3a74a8188609809d04d980c
Source noteuspto-grants-2011_03