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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1456535Generated: October 30, 2026

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

https://huagongshe.com/reaction/1456535

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 numberUS05843949
Source datasetuspto-grants-1998_12
ORD IDord-7ae75bf2e36e46d0881b4ece38b7ec67
Source noteuspto-grants-1998_12