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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223577Generated: October 27, 2026

Hydrochloric Acid → 3-(1-Allyl-4-piperidyl)-1,2-benzisoxazole hydrochloride

https://huagongshe.com/reaction/223577

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium IodideHCID 4875—
ReactantAllyl bromideHCID 7841—
ReactantSodium BicarbonateHCID 516892—
Reactant3-(Piperidin-4-yl)benzo[d]isoxazoleHCID 13076436—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product3-(1-Allyl-4-piperidyl)-1,2-benzisoxazole hydrochlorideHCID 13076451—

Reaction Steps

A suspension of 4.0 g of 3-(4-piperidyl)-1,2-benzisoxazole, 2.6 g of allyl bromide, 5.0 g of sodium bicarbonate, and 3.0 g of potassium iodide in 90 ml of dimethylformamide was stirred at 80° for 20 hrs. The reaction was cooled, filtered and poured into 1 l of water. The mixture was extracted with ether (three times) and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure to give an oil. The oil was dissolved in a small amount of ether into which hydrochloric acid was bubbled. The precipitate was recrystallized from ethanol-ether (three times) to give 2.4 g of product, mp, 174°-176°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04355037
Source datasetuspto-grants-1982_10
ORD IDord-fd4c856bdd334881a85b103538b6656c
Source noteuspto-grants-1982_10