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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835592Generated: October 25, 2026

Potassium Iodide → 4-(Benzyloxy)-2-[(5-methyl-5-cyanohexyl)oxy]-benzophenone

https://huagongshe.com/reaction/1835592

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant4'-Benzyloxy-2'-hydroxyacetophenoneHCID 309257—
Reactant6-Bromo-2,2-dimethylhexanenitrileHCID 4638215—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-(Benzyloxy)-2-[(5-methyl-5-cyanohexyl)oxy]-benzophenoneHCID 23501784111%

Reaction Steps

A solution of 4-benzyloxy-2-hydroxyacetophenone (2.45 g), potassium carbonate (3.25 g), potassium iodide (0.42 g), and 5-cyano-5-methyl-1-bromohexane (2.6 g) in dimethylformamide (40 mL) was heated at 90° C. for 22 hours under nitrogen. The slurry was cooled, poured into water (150 mL) and extracted with ethyl acetate. The combined extracts were washed with water, dried (MgSO4), filtered, and concentrated under reduced pressure to an orange oil. This was purified by flash chromatography (ethyl acetate:hexane) to afford the product (2.4 g) as a clear oil. NMR(CDCl3): 1.37, s (6H); 1.64, m (4H); 1.89, m (2H); 2.58, s (3H); 4.03, t (3H); 5.09, s (2H); 6.50, s (1H); 6.58, d (1H); 7.37, m (5 H); 7.81, d (1H). Mass Spec (GC-MS) m/z=365 (M).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06770259B2
Source datasetuspto-grants-2004_08
ORD IDord-d0a4102658d44d36b5d976d8d75ca7c9
Source noteuspto-grants-2004_08