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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1451021Generated: October 29, 2026

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

https://huagongshe.com/reaction/1451021

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 numberUS05602158
Source datasetuspto-grants-1997_02
ORD IDord-7e7ba2ebd53043368c3649f7b3c62b64
Source noteuspto-grants-1997_02