HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 4-Ethynyl-4-(2-nitrophenoxy)piperidine maleate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Maleic Acid | HCID 444266 | — |
| Reactant | 1-Phenoxycarbonyl-4-ethynyl-4-(2-nitrophenoxy)piperidine | HCID 14281485 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Ethynyl-4-(2-nitrophenoxy)piperidine maleate | HCID 14281487 | 43% |
Reaction Steps
A suspension of 1.00 g of 1-phenoxycarbonyl-4-ethynyl-4-(2-nitrophenoxy)piperidine, 14 ml of methanol, and 6 ml of 15% sodium hydroxide solution was heated at reflux for 2.5 hrs under nitrogen and allowed to cool to room temperature. The mixture was poured into water, extracted twice with chloroform, washed with saturated sodium chloride solution and dried over anhydrous potassium carbonate. Evaporation of solvent provided an oil. Treatment of a solution of the oil which ethereal maleic acid provided 0.43 g (43%) of product, mp 155°-157°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04788201 |
| Source dataset | uspto-grants-1988_11 |
| ORD ID | ord-5dc3dff8b0524d5181fc0bf225e54621 |
| Source note | uspto-grants-1988_11 |