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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351988Generated: November 4, 2026

Sodium hydride → HCID 69456027, compound

https://huagongshe.com/reaction/1351988

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant4-(t-Butyldimethylsilyloxy)indoleHCID 11593976—
ReactantHCID 22916878HCID 22916878—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 69456027HCID 6945602739%

Reaction Steps

Under nitrogen atmosphere, to a suspension of sodium hydride (60% dispersion in mineral oil, 750 mg, 18.8 mmol) in dimethyl-formamide (30 mL) is added dropwise a solution of 4-{[tert-butyl-(dimethyl)silyl]oxy}-1H-indole (2.32 g, 9.38 mmol) in dimethylformamide (10 mL)-with stirring under ice-cooling, and the mixture is stirred at the same temperature for 15 minutes. To the mixture is added dropwise acetonitrile bromide (1.96 mL, 28.1 mmol), and the mixture is stirred at room temperature for 15 hours. The reaction mixture is diluted with a mixture of a saturated brine and water (1:1, 400 mL), and the mixture is extracted with ethyl acetate (2×100 mL). The combined organic layer is washed with a mixture of a saturated brine and water (1:1, 100 mL), dried over anhydrous potassium carbonate, and filtered. The filtrate is concentrated under reduced pressure, and the obtained residue is purified by silica gel column (ethyl acetate:hexane=10:1→5:1) to give the title compound as a pale brown solid (803 mg, yield: 39%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07217724B2
Source datasetuspto-grants-2007_05
ORD IDord-9a13249d5dbd4ee2aba9ed1f4f5d24ba
Source noteuspto-grants-2007_05