Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193553Generated: October 30, 2026

Hydrochloric Acid → 1-N-Ethoxycarbonyl-4-(2-amino-4-fluorophenoxy)-4-ethynylpiperidine

https://huagongshe.com/reaction/1193553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
Reactant1-Ethoxycarbonyl-4-ethynyl-4-(4-fluoro-2-nitrophenoxy)piperidineHCID 14281484—
CatalystIronHCID 23925—
SolventWaterHCID 962—
Product1-N-Ethoxycarbonyl-4-(2-amino-4-fluorophenoxy)-4-ethynylpiperidineHCID 1428149599.4%

Reaction Steps

To a stirred solution of 22.3 g of 1-ethoxycarbonyl-4-ethynyl-4-(4-fluoro-2-nitrophenoxy)piperidine in 535 methanol was added 37 ml of concentrated hydrochloric acid in 150 ml of water. To the stirred mixture was added 78.6 g of iron (reduced, electrolytic) in aliquots. The reaction temperature rose to 45°. The reaction mixture cooled to ambient temperature over 1.5 hr. The mixture was poured into water/ice/sodium carbonate solution, extracted with dichloromethane, washed with water and saturated sodium chloride solution and dried over anhydrous potassium carbonate. Filtration followed by evaporation of solvent provided 20.2 g of an oil. An aliquot of 10.0 g of the oil was dissolved in ether and filtered through 200 g of alumina and the filtrate was evaporated. The residue was dissolved in 10% methanol/dichloromethane, filtered through 200 g of silica gel, and the filtrate was evaporated to provide 8.6 g (84.7%) of product, as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04810792
Source datasetuspto-grants-1989_03
ORD IDord-4aebc1ca12e94a7e8b4e1933cc1970b1
Source noteuspto-grants-1989_03