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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198143Generated: October 30, 2026

Iodoethane → 1-Ethyl-4-nitroxypiperidine fumarate

https://huagongshe.com/reaction/1198143

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 organic 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 numberUS05280031
Source datasetuspto-grants-1994_01
ORD IDord-d36d7f5996b14bccb8ec0ade5a9153fa
Source noteuspto-grants-1994_01