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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1661376Generated: October 29, 2026

Sodium hydride → (2-Methyl-6,7-dihydro-8H-indeno[5,4-d][1,3]oxazol-8-ylidene)acetonitrile

https://huagongshe.com/reaction/1661376

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantDiethyl (cyanomethyl)phosphonateHCID 75676—
Reactant2-Methyl-6,7-dihydro-8H-indeno[5,4-d][1,3]oxazol-8-oneHCID 57781277—
SolventTetrahydrofuranHCID 8028—
Product(2-Methyl-6,7-dihydro-8H-indeno[5,4-d][1,3]oxazol-8-ylidene)acetonitrileHCID 6735341176.3%

Reaction Steps

To a suspension of 60% sodium hydride (90.0 mg, 2.24 mmol) in tetrahydrofuran (9 mL) was added diethyl cyanomethylphosphonate (393 μL, 2.43 mmol) under ice-cooling, and the mixture was stirred for 15 min. Thereto was added a solution of 2-methyl-6,7-dihydro-8H-indeno[5,4-d][1,3]oxazol-8-one (350 mg, 1.87 mmol) in tetrahydrofuran (9 mL), and the mixture was further stirred for 1 hr. To the reaction mixture was added saturated aqueous ammonium chloride solution, and the mixture was extracted with ethyl acetate. The extract was washed with 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=10/90→40/60) to give the title compound (300 mg, yield 76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030337B2
Source datasetuspto-grants-2011_10
ORD IDord-c356615c746d45518f960a20581dcfd4
Source noteuspto-grants-2011_10