Methyl iodide → HCID 20080581, compound
Reaction equation
[F:1][C:2]1[CH:3]=[C:4]([O:15][CH2:16][C:17]2[CH:26]=[CH:25][C:24]3[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=3)[CH:18]=2)[CH:5]=[C:6]([C:8]2([OH:14])[CH2:13][CH2:12][O:11][CH2:10][CH2:9]2)[CH:7]=1.[CH3:27]I>>[F:1][C:2]1[CH:3]=[C:4]([O:15][CH2:16][C:17]2[CH:26]=[CH:25][C:24]3[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=3)[CH:18]=2)[CH:5]=[C:6]([C:8]2([O:14][CH3:27])[CH2:13][CH2:12][O:11][CH2:10][CH2:9]2)[CH:7]=1Participants
3
Procedure
Using the procedure described in Example 3, 4-[5-fluoro-3-(naphth-2-ylmethoxy)phenyl]-4-hydroxytetrahydropyran was reacted with methyl iodide to give 4-[5-fluoro-3-(naphth-2-ylmethoxy)phenyl]-4-methoxytetrahydropyran in 98% yield, m.p. 109°-111° C.
Sources & evidence
- ORD record
- ord-ec11fd3c0e8a4128b328ac245b68ed9f
- Source dataset
- uspto-grants-1995_04
- Patent number
- US05403859
Reaction notes
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