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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2379987Generated: October 30, 2026

Potassium Carbonate → 3-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)1-piperidinyl]-2,2-dimethyl1-propanol fumarate

https://huagongshe.com/reaction/2379987

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-Bromo-2,2-dimethyl-1-propanolHCID 142501—
Reactant3-(4-Piperidyl)-6-fluoro-1,2-benzisoxazoleHCID 849421—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product3-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)1-piperidinyl]-2,2-dimethyl1-propanol fumarateHCID 21960070—

Reaction Steps

A mixture of 4-(6-fluoro-1,2-benzisoxazol-3-yl)piperidine (3.0 gm, 13.6 mmoles), K2CO3 (12.5 gm, 17.5 mmoles), 3-bromo-2,2-dimethyl-1-propanol (3 gm, 21 mmoles, 1.5 eq.), tetrabutylammonium hydrogen sulfate (1 gm, phase transfer catalyst) in water (5 ml) and acetonitrile (150 ml) was heated at reflux for 43 days. TLC showed a small spot for the expected product. The mixture was diluted with EtOAc (400 ml) and washed with brine. The organic solution was dried and concentrated to a dark brown mixture. The crude mixture was purified carefully by flash chromatography (SiO2, 95 gm to afford the dried pure product; 260 mg, (6%) as an oil. This oil was converted to the fumarate salt by treatment with fumaric acid (98.5 mg, 1.0 eq.) in ethanol. Recrystallization from ethanol:ether yielded 210 mg of white crystals, m.p.=144°-145° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05364866
Source datasetuspto-grants-1994_11
ORD IDord-560f68d190ae48768759aad5936bd940
Source noteuspto-grants-1994_11