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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2232329Generated: October 26, 2026

Hydrochloric Acid → 1-Methyl-4-(2-aminophenoxy)-4-ethynylpiperidine

https://huagongshe.com/reaction/2232329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantSodium CarbonateHCID 10340—
Reactant1-Methyl-4-ethynyl-4-(2-nitrophenoxy)piperidineHCID 21272570—
CatalystIronHCID 23925—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product1-Methyl-4-(2-aminophenoxy)-4-ethynylpiperidineHCID 2127259283%

Reaction Steps

A suspension of 1-methyl-4-ethynyl-4-(2-nitrophenoxy)piperidine (liberated from 10.0 g of the hydrochloride), 140 ml of methanol, 40 ml of water, 10 ml of conc hydrochloric acid and 20 g of iron (reduced electroytic) was stirred for 0.5 hr at 45° under nitrogen. The mixture was allowed to cool to room temperature, poured into saturated sodium carbonate solution, extracted twice with ether; dried over anhydrous potassium carbonate, filtered, and the solvent was evaporated to provide an oil. The oil was dissolved in ether. Precipitation with ethereal hydrogen chloride provided 8.59 g (83%) of product. Recrystallization from ethanol provided the analytical sample.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04788201
Source datasetuspto-grants-1988_11
ORD IDord-60bfbc30af0c4248b8c6c69c3f5c7ea0
Source noteuspto-grants-1988_11