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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1780196Generated: October 31, 2026

Chloroacetyl chloride → 1-(2-Chloroacetyl)4-(6-fluoro-1,2-benzisoxazol-3-yl)piperidine

https://huagongshe.com/reaction/1780196

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantTriethylamineHCID 8471—
Reactant3-(4-Piperidyl)-6-fluoro-1,2-benzisoxazoleHCID 849421—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
Product1-(2-Chloroacetyl)4-(6-fluoro-1,2-benzisoxazol-3-yl)piperidineHCID 1846734937.1%

Reaction Steps

A solution of 4-(6-fluoro-1,2-benzisoxazol-3-yl)piperidine (4.4 g, 20 mmol), triethylamine (2.1 g, 21 mmol) in chloroform (50 ml) was added to a solution of chloroacetyl chloride (2.5 g, 22 mmol) in chloroform (100 ml) dropwise at room temperature. The mixture was stirred for 2 hours. The solution was diluted with dichloromethane (DCM, 100 ml) and then washed with H2O and brine. The solvent was removed and the oily product was purified by flash chromatography (SiO2, 50 g; eluted with DCM and 1% CH3OH in DCM). The pure product was obtained as an oil, 4.2 g. Crystallization from ethanol yielded 2.2 g of white crystals, m.p. 101°-102° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05629326
Source datasetuspto-grants-1997_05
ORD IDord-41b09247f4bc4ed19354024f21981d3d
Source noteuspto-grants-1997_05