HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → 1-Ethyl-4-nitroxypiperidine fumarate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Fumarate | HCID 5460307 | — |
| Reactant | HCID 15068866 | HCID 15068866 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1-Ethyl-4-nitroxypiperidine fumarate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05280031 |
| Source dataset | uspto-grants-1994_01 |
| ORD ID | ord-d36d7f5996b14bccb8ec0ade5a9153fa |
| Source note | uspto-grants-1994_01 |