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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248865Generated: October 26, 2026

Chloroacetyl chloride → 1-(2-Chloroacetyl)-4-(2,3,4,5,6-pentafluorophenoxy)piperidine

https://huagongshe.com/reaction/248865

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantTriethylamineHCID 8471—
Reactant4-(2,3,4,5,6-Pentafluorophenoxy)piperidineHCID 14837040—
SolventDichloromethaneHCID 6344—
Product1-(2-Chloroacetyl)-4-(2,3,4,5,6-pentafluorophenoxy)piperidineHCID 19762466—

Reaction Steps

A chilled (ice bath temperature) solution of 10.0 g of 4-(2,3,4,5,6-pentafluorophenoxy)piperidine and 5.72 ml of triethylamine in 100 ml of dichloromethane was treated, dropwise, with a solution of 3.26 ml of chloroacetyl chloride in 40 ml of dichloromethane, and then stirred at room temperature for four hours. The reaction mixture was then washed with water followed by a saturated solution of sodium chloride, dried over anhydrous magnesium sulfate, filtered and concentrated to afford 13.35 g of 1-(2-chloroacetyl)-4-(2,3,4,5,6-pentafluorophenoxy)piperidine as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05212184
Source datasetuspto-grants-1993_05
ORD IDord-3a782f9a998146a1b2148c9002a870a8
Source noteuspto-grants-1993_05