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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 887762Generated: October 31, 2026

Sodium hydride → (1,2-dimethyl-6,7-dihydrocyclopenta[e]indazol-8(2H)-ylidene)acetonitrile

https://huagongshe.com/reaction/887762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantDiethyl (cyanomethyl)phosphonateHCID 75676—
Reactant1,2-dimethyl-6,7-dihydrocyclopenta[e]indazol-8(2H)-oneHCID 59145852—
SolventTetrahydrofuranHCID 8028—
SolventSodium BicarbonateHCID 516892—
Product(1,2-dimethyl-6,7-dihydrocyclopenta[e]indazol-8(2H)-ylidene)acetonitrileHCID 6870135545.2%

Reaction Steps

To a suspension of 60% sodium hydride (58.1 mg, 1.45 mmol) in tetrahydrofuran (4 mL) was added diethyl cyanomethylphosphonate (255 μL, 1.58 mmol), and the mixture was stirred at room temperature for 15 min. A solution of 1,2-dimethyl-6,7-dihydrocyclopenta[e]indazol-8(2H)-one (243 mg, 1.21 mmol) in tetrahydrofuran (8 mL) was added thereto, and the mixture was stirred at 60° C. for 24 hr. The reaction solution was diluted with saturated aqueous sodium hydrogen carbonate solution, 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=30/70→80/20) to give the title compound (122 mg) as a mixture with 1,2-dimethyl-6,7-dihydrocyclopenta[e]indazol-8(2H)-one. The obtained title compound was used for the reaction of Reference Example 28 without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247429B2
Source datasetuspto-grants-2012_08
ORD IDord-3fd9e97e81e74f54bf5db141d5fa49af
Source noteuspto-grants-2012_08