Hydrochloric Acid → 2-[2-(1-Ethylpiperidin-2-yl)ethyl]aniline
Reaction equation
[CH2:1]([N:3]1[CH2:8][CH2:7][CH2:6][CH2:5][CH:4]1[CH2:9][CH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=1[NH:17]C=O)[CH3:2].Cl>CO>[NH2:17][C:12]1[CH:13]=[CH:14][CH:15]=[CH:16][C:11]=1[CH2:10][CH2:9][CH:4]1[CH2:5][CH2:6][CH2:7][CH2:8][N:3]1[CH2:1][CH3:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 1-ethyl-2-(2-formamidophenethyl)piperidine (27.6 g., 0.11 mole), methanol (450 ml.) and concentrated HCl (100 ml.) allowed to stand for 24 hr. provides 2-(2-aminophenethyl)-1-ethylpiperidine, purified by distillation, yield 17.72 g. (69%), b.p. 107° - 128° C./0.1 Torr, nD30° 1.5510.
Workup
- distillationprovides 2-(2-aminophenethyl)-1-ethylpiperidine, purified by distillation, yield 17.72 g
Sources & evidence
- ORD record
- ord-dab487eeffaa4c588adc1451670db76b
- Source dataset
- uspto-grants-1976_12
- Patent number
- US04000143
Reaction notes
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