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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | 1-Ethoxycarbonyl-4-ethynyl-4-(4-fluoro-2-nitrophenoxy)piperidine | HCID 14281484 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-N-Ethoxycarbonyl-4-(2-amino-4-fluorophenoxy)-4-ethynylpiperidine | HCID 14281495 | 99.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04810792 |
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| Source dataset | uspto-grants-1989_03 |
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| ORD ID | ord-4aebc1ca12e94a7e8b4e1933cc1970b1 |
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| Source note | uspto-grants-1989_03 |
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