1-Methyl-2-[2-(2-nitrophenyl)ethenyl]pyridin-1-ium iodide → 2-(2-Aminophenethyl)-1-methylpiperidine

HRID 1974082Notes

Reaction equation

HRID 1974082 reaction equation
[I-].[N+:2]([C:5]1[CH:19]=[CH:18][CH:17]=[CH:16][C:6]=1[CH:7]=[CH:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][N+:10]=1[CH3:15])([O-])=O>[Pt]=O.C(O)C>[NH2:2][C:5]1[CH:19]=[CH:18][CH:17]=[CH:16][C:6]=1[CH2:7][CH2:8][CH:9]1[CH2:14][CH2:13][CH2:12][CH2:11][N:10]1[CH3:15]

Participants

4

Reactant 1

HCID 667604421-Methyl-2-[2-(2-nitrophenyl)ethenyl]pyridin-1-ium iodide

Product 1

HCID 110852822-(2-Aminophenethyl)-1-methylpiperidineYield 87%

Reagents, catalysts & solvents 2

HCID 82844Platinum oxide (PtO)CatalystHCID 702EthanolSolvent

Procedure

A suspension of 2-(o-nitrostyryl)-1-methylpyridinium iodide (40.5 mg., 0.11 mole) prepared according to the method of L. Horwitz, J. Org. Chem., 21, 1039 (1956) in 200 ml. of ethanol is hydrogenated in a Parr hydrogenation apparatus employing 0.3 g. of platinum oxide catalyst while maintaining a reaction temperature of from about 50° to 75° C. When the hydrogen uptake ceases (about 3 hours), the reduction mixture is filtered, the filtrate evaporated and the resulting residue taken up in 500 ml. of water. The aqueous solution is basified with 40% sodium hydroxide and extracted with several 200 ml. portions of ether. Ethereal extracts are combined, washed with water, dried over magnesium sulfate, and the ether evaporated. Distillation of the resiude thus obtained provides 20.8 g. (87% yield) of 2-(o-aminophenethyl)-1-methylpiperidine base having a boiling point of 121°-125° C. at 0.04 mm.

Workup

  1. customprepared
  2. filtrationWhen the hydrogen uptake ceases (about 3 hours), the reduction mixture is filtered
  3. customthe filtrate evaporated
  4. extractionextracted with several 200 ml
  5. washwashed with water
  6. dry with materialdried over magnesium sulfate
  7. customthe ether evaporated
  8. distillationDistillation of the resiude
  9. customthus obtained
  10. customprovides 20.8 g

Sources & evidence

ORD record
ord-c4a787a2f61340d7b8f7d316d1fc5ece
Source dataset
uspto-grants-1976_12
Patent number
US04000143

Reaction notes

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