Isopropyl iodide → Ethyl 2,6-bis(trifluoromethyl)-4-isopropoxy-3-pyridinecarboxylate
Reaction equation
[F:1][C:2]([F:20])([F:19])[C:3]1[C:8]([C:9]([O:11][CH2:12][CH3:13])=[O:10])=[C:7]([OH:14])[CH:6]=[C:5]([C:15]([F:18])([F:17])[F:16])[N:4]=1.I[CH:22]([CH3:24])[CH3:23]>>[F:20][C:2]([F:19])([F:1])[C:3]1[C:8]([C:9]([O:11][CH2:12][CH3:13])=[O:10])=[C:7]([O:14][CH:22]([CH3:24])[CH3:23])[CH:6]=[C:5]([C:15]([F:18])([F:17])[F:16])[N:4]=1Participants
3
Procedure
Following the procedure of Example 4, this material was prepared in 74% yield from product of Example 2 and 2-iodopropane as a liquid, nD25 1.4210.
Sources & evidence
- ORD record
- ord-b4ef8a20a7f04e1fa585da3010cd7926
- Source dataset
- uspto-grants-1989_05
- Patent number
- US04835279
Reaction notes
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