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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1069313Generated: October 29, 2026

Potassium Carbonate → 4-(6-Fluoro-1,2-benzisoxazoi-3-yl)-1-(2'-methoxyphenyl)butylpiperidine maleate

https://huagongshe.com/reaction/1069313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantMaleic AcidHCID 444266—
Reactant3-(4-Piperidyl)-6-fluoro-1,2-benzisoxazoleHCID 849421—
Reactant1-(4-Bromobutyl)-2-methoxybenzeneHCID 19072468—
SolventEthanolHCID 702—
SolventAcetonitrileHCID 6342—
Product4-(6-Fluoro-1,2-benzisoxazoi-3-yl)-1-(2'-methoxyphenyl)butylpiperidine maleateHCID 86748255—

Reaction Steps

A mixture of 6-fluoro-3-(4-piperidinyl)-1,2-benzisoxazole (2.36 g, 10.7 mmole), K2CO3 (2 g, 14.5 mmol) and 2-(4-bromobutyl)anisole (2.4 g, 10 mmol) in acetonitrile (100 ml) was heated at reflux for 2.5 hours. At the end of reaction, the solvent was removed. The residue was extracted into dichloromethane (200 ml) and filtered. The dichloromethane solution was concentrated. The crude oil obtained was purified on a flash chromatography column. The material thus purified was a light yellow oil (2.73 g, 53%). This oil was dissolved in ethanol and treated with maleic acid (607 mg, 1.0 eq) in ethanol. The 4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-(2′-methoxyphenyl)butylpiperidine maleate crystals formed on concentration and subsequent cooling to 0° C. These were collected and dried to yield 2.05 g, m.p.=132-133° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06251907B1
Source datasetuspto-grants-2001_06
ORD IDord-edcc4f2ec68c403c9a1242f865908af7
Source noteuspto-grants-2001_06