2-Thiophenecarboxaldehyde → HCID 59054377, compound
Reaction equation
[Cl:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH:5]=[CH:4][C:3]=1[O:12][CH:13]([CH3:16])[CH2:14][NH2:15].[S:17]1[CH:21]=[CH:20][CH:19]=[C:18]1[CH:22]=O>>[Cl:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH:5]=[CH:4][C:3]=1[O:12][CH:13]([CH3:16])[CH2:14][NH:15][CH2:22][C:18]1[S:17][CH:21]=[CH:20][CH:19]=1Participants
3
Procedure
Prepared from 2-[(1-chloronaphthalen-2-yl)oxy]propan-1-amine and thiophen-2-carbaldehyde in 81% yield as a pale yellow oil.
Sources & evidence
- ORD record
- ord-2fabcd69af9542f983647c6d93fc13e5
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08906946B2
Reaction notes
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