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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 887761Generated: October 25, 2026

Sodium hydride → (2-methyl-6,7-dihydrocyclopenta[e]indazol-8(2H)-ylidene)acetonitrile

https://huagongshe.com/reaction/887761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantDiethyl (cyanomethyl)phosphonateHCID 75676—
Reactant2-methyl-6,7-dihydrocyclopenta[e]indazol-8(2H)-oneHCID 59145926—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(2-methyl-6,7-dihydrocyclopenta[e]indazol-8(2H)-ylidene)acetonitrileHCID 6869957968%

Reaction Steps

To a suspension of 60% sodium hydride (116 mg, 2.90 mmol) in tetrahydrofuran (8 mL) was added diethyl cyanomethylphosphonate (516 μL, 3.19 mmol), and the mixture was stirred at room temperature for 30 min. A solution of 2-methyl-6,7-dihydrocyclopenta[e]indazol-8(2H)-one (180 mg, 0.97 mmol) in tetrahydrofuran (2 mL) was added thereto, and the mixture was stirred at 50° C. for 30 min. The reaction solution was diluted with water, extracted with ethyl acetate, washed with water and saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane=35/65→70/30) to give the title compound (138 mg, yield 68%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247429B2
Source datasetuspto-grants-2012_08
ORD IDord-d2e72fb199db4e8590cf0c345527a6e8
Source noteuspto-grants-2012_08