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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223576Generated: October 30, 2026

Potassium Iodide → 3-(1-Allyl-4-piperidyl)-6-chloro-1,2-benzisoxazole hydrochloride

https://huagongshe.com/reaction/223576

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium ChlorideHCID 5234—
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
Reactant6-Chloro-3-(piperidin-4-yl)benzo[d]isoxazoleHCID 13076430—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product3-(1-Allyl-4-piperidyl)-6-chloro-1,2-benzisoxazole hydrochlorideHCID 13076449127.7%

Reaction Steps

A suspension of 3.55 g of 3-(4-piperidyl)-6-chloro-1,2-benzisoxazole, 2.0 g of allyl bromide, 2.0 g of potassium carbonate and some crystals of potassium iodide in 47 ml of dimethylformamide was stirred under nitrogen at 85°-90° for 5 hrs. The reaction mixture was cooled and filtered. The crystals were washed with dichloromethane. The combined organic solvents (dimethylformamide+dichloromethane) were distilled in vacuo and to the residue was added with 30 ml ethanol and 500 ml half-saturated sodium chloride, prepared by diluting saturated sodium chloride with an equal volume of water. After 16 hrs, the crystals were filtered, washed with water and dried, yielding base. The base was dissolved in 50 ml of ethanol and 1.2 ml of conc hydrochloric acid. The mixture was heated to 50°. The solvents were evaporated in vacuo. Benzene (60 ml) was added and distilled in vacuo. The residue was triturated with ether, filtered and twice recrystallized from isopropanol-ether, giving 3.0 g (63.9%) of product as the hydrochloride, mp, 178°-180°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04355037
Source datasetuspto-grants-1982_10
ORD IDord-813a3cd341d545d5b4b40bdf31745fbd
Source noteuspto-grants-1982_10