3-(3-Chlorophenyl)-2-propynal → 3-(3-Chlorophenyl)prop-2-ynal oxime
Reaction equation
[C:1]1([C:7]#[C:8][CH:9]=[N:10][OH:11])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Cl:12]C1C=C(C#CC=O)C=CC=1>>[Cl:12][C:3]1[CH:2]=[C:1]([C:7]#[C:8][CH:9]=[N:10][OH:11])[CH:6]=[CH:5][CH:4]=1Participants
3
Procedure
The title compound was prepared following the method here described for Compound 1a, using Compound 31d instead of phenylpropiolaldehyde. The pale brown residue was used in the next step without further purification. Yield: 96.4%.
Workup
- customThe pale brown residue was used in the next step without further purification
Sources & evidence
- ORD record
- ord-a3b51d3f27f14f879e822be58fb81423
- Source dataset
- uspto-grants-2013_11
- Patent number
- US08580962B2
Reaction notes
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