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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086490Generated: October 31, 2026

Iodoethane → 1-Ethyl-4-nitroxypiperidine fumarate

https://huagongshe.com/reaction/1086490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantPotassium CarbonateHCID 11430—
ReactantFumarateHCID 5460307—
ReactantHCID 15068866HCID 15068866—
SolventAcetoneHCID 180—
Product1-Ethyl-4-nitroxypiperidine fumarateHCID 86744896—

Reaction Steps

6.9 g. 4-Nitroxypiperidine are dissolved in 50 ml. acetone, mixed with 13.8 g. potassium carbonate and 6.1 ml. ethyl iodide and stirred for 18 hours at ambient temperature. After filtering with suction, the filtrate is evaporated, the residue is dissolved in ethyl acetate and extracted twice with aqueous sodium chloride solution. The orgainc phase is dried with anhydrous sodium sulphate. The crude product (8.2 g.) remaining after suction filtration and evaporation is converted into the fumarate by dissolving in ethanol and adding 2.7 g. fumaric acid. After filtering off with suction, there are obtained 2.6 g. of the fumarate of the title compound, i.e. 23% of theory; m.p. 131°-134° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05030641
Source datasetuspto-grants-1991_07
ORD IDord-b2dab2d39ef8479eacbbd4585a6d4e18
Source noteuspto-grants-1991_07