Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193551Generated: October 27, 2026

Ethyl chloroformate → 1-Ethoxycarbonyl-4-ethynyl-4-(4-fluoro-2-nitrophenoxy)piperidine

https://huagongshe.com/reaction/1193551

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantPotassium CarbonateHCID 11430—
ReactantN-Methyl-4-ethynyl-4-(4-fluoro-2-nitrophenoxy)piperidineHCID 14281483—
SolventBenzeneHCID 241—
Product1-Ethoxycarbonyl-4-ethynyl-4-(4-fluoro-2-nitrophenoxy)piperidineHCID 1428148483.9%

Reaction Steps

A suspension of 223 g of N-methyl-4-ethynyl-4-(4-fluoro-2-nitrophenoxy)piperidine, 2 l of dry benzene, 165 g of anhydrous potassium carbonate and 130.3 g of ethyl chloroformate was stirred at reflux for 18 hr under nitrogen. The mixture was filtered and the solvent evaporated. The residue was dissolved in ether, washed with hydrochloric acid, saturated sodium bicarbonate solution, water and saturated sodium chloride solution. The ether solution was dried over anhydrous sodium sulfate and filtered. Evaporation of solvent provided an oil, which was dried at 50°-55° (1 mm). The oil crystallized to provide 226 g (83.8%) of product, mp 56°-68°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04810792
Source datasetuspto-grants-1989_03
ORD IDord-a6ecdb2cdda444788afe8d7659f403d1
Source noteuspto-grants-1989_03