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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1847951Generated: October 31, 2026

Water → HCID 50993163, compound

https://huagongshe.com/reaction/1847951

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantIsobutanolHCID 6560—
ReactantSodium hydrideHCID 24758—
Reactant2-Fluoro-5-iodobenzonitrileHCID 2778928—
SolventDimethylformamideHCID 6228—
ProductHCID 50993163HCID 5099316378.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 2-methyl-1-propanol (0.56 mL, 6.06 mmol) in N,N-dimethylformamide (10 mL) was cooled to 0° C. and to this was added sodium hydride (242 mg, a 60% suspension in mineral oil, 6.06 mmol) in small portions. The turbid reaction mixture was stirred at 0° C. for 5 minutes and the temperature was raised to 23° C. Thereafter, the mixture was stirred at room temperature for 10 minutes and cooled again to 0° C. To the reaction mixture was added 2-fluoro-5-iodobenzonitrile (1.0 g, 4.04 mmol) and, after being warmed to room temperature, the reaction mixture was stirred for 1.5 hours. After the reaction was complete, water (20 mL) was added to the reaction mixture, which was extracted with ethyl acetate (3×30 mL). The organic phases were combined, washed with a saturated aqueous sodium chloride solution (3×30 mL), and thereafter dried over anhydrous magnesium sulfate. After removing magnesium sulfate by filtration, the solvent was concentrated under reduced pressure. The crude product obtained was purified by silica gel chromatography (hexane/ethyl acetate=98/2) to obtain the title compound (950 mg). Yield, 78%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952174B2
Source datasetuspto-grants-2015_02
ORD IDord-18c93e41a7594a27af3ce4e52e56ac9a
Source noteuspto-grants-2015_02