Pyrrole-2-carboxaldehyde → HCID 86652339, compound
Reaction equation
[NH:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[CH:6]=[O:7].Br[CH2:9][CH2:10][O:11][Si:12]([C:15]([CH3:18])([CH3:17])[CH3:16])([CH3:14])[CH3:13]>>[CH3:9][CH2:10][O:11][Si:12]([C:15]([CH3:18])([CH3:17])[CH3:16])([CH3:14])[CH3:13].[NH:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[CH:6]=[O:7]Participants
3
Procedure
1H-Pyrrole-2-carbaldehyde was alkylated with (2-bromoethoxy)(tert-butyl)dimethylsilane as described in Example 12, step 1 to provide 1-(2-ethoxy-tert-butyldimethylsilane-1H-pyrrole-2-carbaldehyde as a light yellow oil.
Sources & evidence
- ORD record
- ord-213bf511257e4a5aa8e32e04651ff003
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08906954B2
Reaction notes
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