Iodoethane → Ethyl 2,6-bis(trifluoromethyl)-4-ethoxy-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.[CH2:21](I)[CH3:22]>>[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][CH2:21][CH3:22])[CH:6]=[C:5]([C:15]([F:18])([F:17])[F:16])[N:4]=1Participants
3
Procedure
This material was prepared following the procedure of Example 4 in 77% yield from product of Example 2 and ethyl iodide as a white solid; mp 57°-59° C.
Workup
- customThis material was prepared
Sources & evidence
- ORD record
- ord-0ad93d851df94e46a26cdc48d38355a8
- Source dataset
- uspto-grants-1989_01
- Patent number
- US04797149
Reaction notes
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