Methyl iodide → HCID 21657770, compound
Reaction equation
[CH2:1]([CH:3]1[CH2:8][C:7]([OH:26])([C:9]2[CH:14]=[CH:13][CH:12]=[C:11]([S:15][C:16]3[CH:21]=[CH:20][C:19]([C:22]([CH3:25])([CH3:24])[CH3:23])=[CH:18][CH:17]=3)[CH:10]=2)[CH2:6][CH2:5][O:4]1)[CH3:2].[CH3:27]I>>[CH2:1]([CH:3]1[CH2:8][C:7]([O:26][CH3:27])([C:9]2[CH:14]=[CH:13][CH:12]=[C:11]([S:15][C:16]3[CH:17]=[CH:18][C:19]([C:22]([CH3:25])([CH3:24])[CH3:23])=[CH:20][CH:21]=3)[CH:10]=2)[CH2:6][CH2:5][O:4]1)[CH3:2]Participants
3
Procedure
Using a similar procedure to that described in Example 3, (2RS,4SR)-2-ethyl-4-hydroxy-4-[3-(4-tert-butylphenylthio)phenyl]tetrahydropyran was reacted with methyl iodide to give (2RS,4SR)-2-ethyl-4-methoxy-4-[3-(4-tert-butylphenylthio)phenyl]tetrahydropyran in 43% yield as an oil.
Sources & evidence
- ORD record
- ord-83118c2eabce435db470c58945bdec72
- Source dataset
- uspto-grants-1993_05
- Patent number
- US05208259
Reaction notes
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