N-Hydroxy-3-trimethylsilyl-prop-2-ynimidoyl chloride → N-hydroxy-3-(m-tolyl)prop-2-ynimidoyl chloride
Reaction equation
[OH:1][N:2]=[C:3]([Cl:10])[C:4]#[C:5][Si](C)(C)C.ON=CC#[C:15][C:16]1[CH:21]=[CH:20][CH:19]=[C:18](C)[CH:17]=1>>[OH:1][N:2]=[C:3]([Cl:10])[C:4]#[C:5][C:18]1[CH:17]=[C:16]([CH3:15])[CH:21]=[CH:20][CH:19]=1Participants
3
Procedure
The title compound was prepared following the method herein described for Compound 3b, using Compound 91c instead of 3-trimethylsilylprop-2-ynal oxime. The residue was used in the next step without further purification. Yield: 96.4%.
Workup
- customThe residue was used in the next step without further purification
Sources & evidence
- ORD record
- ord-9aba6ff3f2f147f7b09a5ba1475bd47a
- Source dataset
- uspto-grants-2013_11
- Patent number
- US08580962B2
Reaction notes
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