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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503196Generated: October 30, 2026

Sodium Iodide → HCID 11132285, compound

https://huagongshe.com/reaction/1503196

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantPotassium CarbonateHCID 11430—
Reactant4-HydroxybenzophenoneHCID 14347—
SolventMethyl Ethyl KetoneHCID 6569—
ProductHCID 11132285HCID 1113228590.1%

Reaction Conditions

Temperature70 °C

Reaction Steps

A 1000 mL three-neck flask was charged with 4-hydroxybenzophenone (50.00 g; 252.2 mmol), 1-bromo-3-chloropropane (79.41 g; 504.4 mmol) and 2-butanone (500 mL). After flushing with nitrogen, anhydrous potassium carbonate (104.6 g; 756.5 mmol) was added and the reaction mixture was stirred at reflux for 24 h. Full consumption of the starting 4-hydroxybenzophenone was confirmed by TLC. The reaction mixture was filtered, the filtrate evaporated, the oily residue dissolved in dichloromethane (300 mL) and extracted with water (3×100 mL). The organic phase was separated, evaporated, and the unreacted 1-bromo-3-chloropropane was removed by heating to 70° C. in vacuo. The residue was dissolved in 2-butanone (500 mL) and sodium iodide (45.36 g; 302.6 mmol) was added. The reaction mixture was refluxed for 6 h. The reaction mixture was filtered, the filtrate evaporated, the oily residue dissolved in dichloromethane (300 mL) and extracted with water (3×100 mL). The organic phase was separated, evaporated, the light brown oily residue dried in vacuo to give crude 4-(3-iodopropoxyl)benzophenone (light brown solid; 83.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212160B2
Source datasetuspto-grants-2015_12
ORD IDord-c3a3a075342a4eafb2f8797abee23949
Source noteuspto-grants-2015_12