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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 233143Generated: October 25, 2026

Potassium Carbonate → 1-[2-[3-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)1-piperidinyl]propoxy]-5-methylphenyl]ethanone

https://huagongshe.com/reaction/233143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-[2-(3-Bromopropoxy)-5-methylphenyl]ethanoneHCID 10423299—
ReactantR-56109 hydrochlorideHCID 11334359—
SolventDimethylformamideHCID 6228—
SolventAcetonitrileHCID 6342—
Product1-[2-[3-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)1-piperidinyl]propoxy]-5-methylphenyl]ethanoneHCID 1047668146.2%

Reaction Conditions

Temperature95 °C

Reaction Steps

A mixture of 6-fluoro-3-(4-piperidinyl)-l,2-benzisoxazole hydrochloride (2.87 g, 11.23 mmol), K2CO3 (2.5 g), 1-[2-(3-bromopropoxy)-5-methylphenyl]ethanone (3.74 g, 13.8 mmol) in dimethylformamide (10 ml) and acetonitrile (50 ml) was heated at 95° C. for 6 hours. At the end of the reaction, the solvent was concentrated and the mixture was extracted into dichloromethane (300 ml). The organic solution was washed with water and brine, dried over MgSO4, then concentrated down to a crude oil. The purification was done by flash chromatography over a silica gel column (SiO2, 60 g, eluted with 1% CH3OH:dichloromethane: 1.2 l; 3% CH3OH:dichloromethane: 600 ml). The material thus obtained was crystallized from a small volume of ether and hexane to provide 2.13 g (46%) of off-white 1-[2-[3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propoxy]-5-methylphenyl]ethanone, m.p.=92°-93° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05591745
Source datasetuspto-grants-1997_01
ORD IDord-6a1d52f15cab46ee85bac83d9a261f7b
Source noteuspto-grants-1997_01