1-Benzyl-4-(naphthalen-2-yloxy)piperidine → 4-(5-Fluoro-1-naphthalenyloxy)piperidine
Reaction equation
[F:1][C:2]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][CH:6]=[C:7]2[O:12][CH:13]1[CH2:18][CH2:17][N:16](CC)[CH2:15][CH2:14]1.C1C2C(=CC=CC=2)C=CC=1OC1CCN(CC2C=CC=CC=2)CC1>>[F:1][C:2]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][CH:6]=[C:7]2[O:12][CH:13]1[CH2:14][CH2:15][NH:16][CH2:17][CH2:18]1Participants
3
Procedure
When in the procedure of Example 7, 4-(5-fluoro-1-naphthalenyloxy)-1-ethylpiperidine is substituted for 4-(2-naphthalenyloxy)-1-(phenylmethyl)piperidine, 4-(5-fluoro-1-naphthalenyloxy)piperidine is produced.
Sources & evidence
- ORD record
- ord-3d1b9f810b394731a2ec47749db8902e
- Source dataset
- uspto-grants-1984_04
- Patent number
- US04443462
Reaction notes
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