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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2184549Generated: October 29, 2026

Dichloromethane → 4-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]butyl decanoate fumarate

https://huagongshe.com/reaction/2184549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
ReactantFumaric AcidHCID 444972—
Reactant4-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]butanolHCID 21960038—
SolventEthanolHCID 702—
Product4-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]butyl decanoate fumarateHCID 21960009—

Reaction Steps

To a solution of 4-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]butanol (2.0 g, 6.84 mmol), triethylamine (1.0 g, 10 mmol) in DCM (70 ml) decanoyl chloride (1.7 g, 8.9 mmol) was added dropwise at room temperature. The mixture was stirred for 1 hour., then was concentrated to a crude solid. The solid was extracted into ethyl acetate, and the insoluble salts were filtered. The solvents were removed. The crude product was purified by flash chromatography (Sorbsil C-30, 30 g, eluted with a mixture of MeOH in DCM). The oil thus obtained (2.5 g, 81%) was converted to a fumarate salt with fumaric acid (650 mg, 1.0 eq) in ethanol. Crystals were collected: 1.48 g, m.p.=109°-110° C. ANALYSIS: Calculated for C20H39FN2O3.C4H4O4: 64.04%C 7.70%H 4.98%N Found: 64.30%C 7.86%H 4.78%N

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE037729E1
Source datasetuspto-grants-2002_06
ORD IDord-7afa577b56704f75a3488682af4e261d
Source noteuspto-grants-2002_06