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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113642Generated: October 30, 2026

Allyl iodide → HCID 12045757, compound

https://huagongshe.com/reaction/2113642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl iodideHCID 11166—
ReactantSodium hydrideHCID 24758—
Reactant2-Butyl-5-methoxy-1-indanoneHCID 12045752—
SolventDimethylformamideHCID 6228—
ProductHCID 12045757HCID 12045757—

Reaction Steps

A solution of 2-butyl-5-methoxy-1-indanone (500 mg, 2.3 mmol) in anhydrous N,N-dimethylformamide (DMF, 5 mL) was added to a suspension of sodium hydride (100 mg of a 60% dispersion in mineral oil, 2.5 mmol) in DMF (5 mL). The mixture was diluted with more DMF (2 mL, used to rinse in the indanone solution), placed under a nitrogen atmosphere, and stirred at room temperature for 25 minutes. Allyl iodide (0.32 mL, 3.5 mmol) was then added over 5 minutes, during which time the mixture clarified. After stirring at room temperature for an additional 15.5 hours, the mixture was partitioned between EtOAc (200 mL) and water (150 mL) containing brine. The aqueous phase was extracted with EtOAc (2×100 mL). The combined EtOAc solution was washed with brine, dried over MgSO4, filtered, and concentrated under vacuum to afford an oil. The crude product was purified by Biotage™ (Charlottesville, Va.) flash chromatography on a 40S (4.0×7.0 cm) silica gel column, eluting with 49:1 hexanes-EtOAc. The product-containing fractions were evaporated under vacuum to afford 2-allyl-2-butyl-5-methoxy-1-indanone as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432284B2
Source datasetuspto-grants-2008_10
ORD IDord-d9bb6cd38a26403dbc2dfd34de2237dd
Source noteuspto-grants-2008_10