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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583435Generated: October 31, 2026

Potassium Iodide → 2-[6-(Quinolin-3-yl)hexyl]-1H-isoindole-1,3(2H)-dione

https://huagongshe.com/reaction/1583435

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant3-(6-Chlorohexyl)quinolineHCID 20260594—
ReactantPhthalimide potassium saltHCID 24194345—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-[6-(Quinolin-3-yl)hexyl]-1H-isoindole-1,3(2H)-dioneHCID 1355755582.4%

Reaction Conditions

Temperature130 °C

Reaction Steps

A solution of 7.8 g of 3-quinolinehexanol in 35 ml of dry dichloromethane was treated dropwise with a solution of 6.07 g of thionyl chloride in 15 ml of dichloromethane. The reaction mixture was heated to reflux for 1 hour and evaporated to dryness. The residue was dissolved in dichloromethane, washed successively with water, saturated sodium bicarbonate solution and brine, dried over potassium carbonate and evaporated to give 8.3 g of crude 6-(3-quinolinyl)hexylchloride. A suspension of 8.3 g of 6-(3-quinolinyl)hexylchloride, 12.6 g of potassium phthalimide, and 0.50 g of potassium iodide in 60 ml of dimethylformamide was heated to a bath temperature of 130° C. for one hour. The cooled mixture was diluted with water and extracted with dichloromethane. The combined organic layers were washed with water, dried over potassium carbonate and evaporated. The crude solid was crystallized from ethyl acetate-hexane to give 9.9 g (82%) of 2-[6-(3-quinolinyl)hexyl]-1H-isoindole-1,3-(2H)-dione, mp 90°-91° C. An analytical sample was obtained from toluene, mp 95.5°-96.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04551460
Source datasetuspto-grants-1985_11
ORD IDord-518d8c847a6041faad2b4806ca7f7c40
Source noteuspto-grants-1985_11