5-Bromosalicylic acid → 5-Cyano-2-isopropoxybenzoic acid
Reaction equation
[C:1]([C:3]1[CH:4]=[C:5]([CH:9]=[C:10](OC(C)C)[CH:11]=1)[C:6]([OH:8])=[O:7])#[N:2].BrC1C=[CH:19][C:20]([OH:26])=[C:21](C=1)C(O)=O>>[C:1]([C:3]1[CH:11]=[CH:10][C:9]([O:26][CH:20]([CH3:21])[CH3:19])=[C:5]([CH:4]=1)[C:6]([OH:8])=[O:7])#[N:2]Participants
3
Procedure
Prepared in an analogous fashion to 3-cyano-5-isopropoxybenzoic acid starting from 5-bromo-2-hydroxybenzoic acid. LCMS-ESI (m/z) calculated for C11H11NO3: 205.2; found 206.1 [M+H]+, tR=2.70 min.
Sources & evidence
- ORD record
- ord-655d40f0fa684d1a8849abc2628cd3b7
- Source dataset
- uspto-grants-2013_01
- Patent number
- US08362048B2
Reaction notes
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