HCID 13787828, compound → HCID 12929196, compound
Reaction equation
[CH3:1][N:2]1[CH2:7][CH:6]([CH3:8])[C:5]([CH2:17][CH2:18][CH3:19])([C:9]2[CH:14]=[CH:13][CH:12]=[C:11]([O:15][CH3:16])[CH:10]=2)[CH2:4][CH2:3]1>C(O)(=O)C>[CH3:1][N:2]1[CH2:7][CH:6]([CH3:8])[C:5]([CH2:17][CH2:18][CH3:19])([C:9]2[CH:14]=[CH:13][CH:12]=[C:11]([O:15][CH3:16])[CH:10]=2)[CH:4]=[CH:3]1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
Following the procedure set forth in Example 1, 43 g. of 1,5-dimethyl-4-n-propyl-4-(3-methoxyphenyl)piperidine was reacted with 276 g. of mercuric acetate in 717 ml. of five percent aqueous acetic acid to provide, after purification by distillation, 30.2 g. of 1,5-dimethyl-4-n-propyl-4-(3-methoxyphenyl)-1,4,5,6-tetrahydropyridine. B.P. 126°-138° C. at 0.15 torr.
Workup
- customafter purification
- distillationby distillation, 30.2 g
Sources & evidence
- ORD record
- ord-986ee712030a46f6bf860f427e3e9e3c
- Source dataset
- uspto-grants-1980_10
- Patent number
- US04228288
Reaction notes
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