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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196583Generated: October 30, 2026

Sodium Iodide → HCID 19786559, compound

https://huagongshe.com/reaction/1196583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant4-(4-Chlorophenyl)-4-hydroxypiperidineHCID 38282—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 19786584HCID 19786584—
SolventDimethylformamideHCID 6228—
ProductHCID 19786559HCID 1978655932.3%

Reaction Steps

To a solution consisting of 5-(3-chloropropyl)-6,7-dihydro-3-phenyl-1,2-benzisoxazol-4(5H)-one (5.02 g) and DMF (170 ml) was added diisopropylethyl amine (7.50 ml), 4-(4-chlorophenyl)-4-hydroxypiperidine (4.03 g) and sodium iodide (2.59 g) at room temperature with stirring. The reaction was flushed with nitrogen and warmed to 78°-80° C. for 11 hours. Upon cooling to room temperature, water and ethyl acetate were added to the reaction mixture. The layers were separated and the aqueous layers extracted three times with ethyl acetate. The combined organic layers were washed with brine and dried (MgSO4). Filtration and concentration gave the crude amine product. Purification via flash chromatography (silica gel, 2% Et3N/ether) afforded 2.60 g of the desired product as an oil. Addition of ether, heat, and slow evaporation gave a powder. The ether was then decanted and the powder was washed with pentane to yield 5-[3-(4-(4-chlorophenyl)-4-hydroxy-piperidinyl)-propyl]-6,7-dihydro-3-phenyl-1,2-benzisoxazol- 4(5H)-one, m.p. 147°-148° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05114936
Source datasetuspto-grants-1992_05
ORD IDord-7131c539da104a638e6be96fa177b064
Source noteuspto-grants-1992_05