HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → N-{2-[2-(1-Ethylpiperidin-2-yl)ethyl]phenyl}formamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-Ethyl-2-[2-(2-formamidophenyl)ethyl]pyridin-1-ium iodide | HCID 20560050 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-{2-[2-(1-Ethylpiperidin-2-yl)ethyl]phenyl}formamide | HCID 20559971 | — |
Reaction Steps
To a solution of 1-ethyl-2-(o-formamidophenethyl)pyridinium iodide (44.8 g., 0.117 mole), 50% NaOH (11.2 g., 0.14 mole), and water (40 ml.) in methanol (330 ml.) is added portionwise NaBH4 (5.32 g., 0.14 mole). The solution is stirred for 2 hr. and evaporated. Water is added to the residue thus obtained and the mixture extracted with ether. The ethereal extracts are dried (MgSO4) and evaporated. The residue taken up in 200 ml. of ethanol and hydrogenated in a Parr apparatus using 5 g. of 10% palladium on carbon as catalyst affords 1-ethyl-2-(2-formamidophenethyl)piperidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04064254 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-d84f4b5a799a43acade4aa4e3bc626b5 |
| Source note | uspto-grants-1977_12 |