1,1,1-Trifluoro-2-iodoethane → Methyl 3-formyl-4,5-dimethyl-1-(2,2,2-trifluoroethyl)pyrrole-2-carboxylate
Reaction equation
[CH:1]([C:3]1[C:7]([CH3:8])=[C:6]([CH3:9])[NH:5][C:4]=1[C:10]([O:12][CH3:13])=[O:11])=[O:2].[F:14][C:15]([F:19])([F:18])[CH2:16]I>>[CH:1]([C:3]1[C:7]([CH3:8])=[C:6]([CH3:9])[N:5]([CH2:16][C:15]([F:19])([F:18])[F:14])[C:4]=1[C:10]([O:12][CH3:13])=[O:11])=[O:2]Participants
3
Procedure
The title compound was prepared as pale brown crystals in 5.5% yeild in a similar procedure to that described in Referential Example 9 by using methyl 3-formyl-4,5-dimethylpyrrole-2-carboxylate and 1,1,1-trifluoro-2-iodoethane.
Sources & evidence
- ORD record
- ord-8aaa2929de4d4918b72a8a0ff2bed6f2
- Source dataset
- uspto-grants-2000_05
- Patent number
- US06063782
Reaction notes
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