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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726862Generated: November 1, 2026

Sodium Chloride → HCID 68827798, compound

https://huagongshe.com/reaction/1726862

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantPhenylacetonitrileHCID 8794—
ReactantHomoallyl bromideHCID 21241—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 68827798HCID 68827798—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-phenylacetonitrile (1 mL) in DMF (1.0 mL) at 0° C. was added sodium hydride (95% oil dispersion, 547 mg) and the resulting suspension was stirred at 0° C. for 10 min. 4-Bromobut-1-ene (2.2 mL) was added, and the reaction mixture was stirred at room temperature for 2 h. Saturated sodium chloride was added followed by ethyl acetate, the aqueous layer was extracted with ethyl acetate. The combined organic layers were dried over anhydrous sodium sulfate and filtered, and the filtrate was evaporated in vacuo. The residue was purified by silica gel flash chromatography eluting with 10% ethyl acetate/90% hexanes to give the title compound as an oil (773 mg). 1H NMR (400 MHz, CDCl3) δ 1.8-2.3 (8H, m), 4.95 (4H, m), 5.73 (2H, m), and 7.31 (5H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07494986B2
Source datasetuspto-grants-2009_02
ORD IDord-6ae3ebdf9f574a7c830ba35a6c506e39
Source noteuspto-grants-2009_02