2-Thiophenecarboxaldehyde → HCID 59054438, 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][CH2:13][CH:14]([NH2:16])[CH3:15].[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][CH2:13][CH:14]([NH:16][CH2:22][C:18]1[S:17][CH:21]=[CH:20][CH:19]=1)[CH3:15]Participants
3
Procedure
Prepared from 1-[(1-chloronaphthalen-2-yl)oxy]propan-2-amine and thiophen-2-carbaldehyde in 62% yield as a pale yellow oil.
Sources & evidence
- ORD record
- ord-807f2eb55b654e228e342210e17cb76b
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08906946B2
Reaction notes
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