Tempo → (E)-1-(3-(Benzyloxy)phenyl)but-2-en-1-one
Reaction equation
[CH2:1]([O:8][C:9]1[CH:10]=[C:11]([CH:15]([OH:19])/[CH:16]=[CH:17]/[CH3:18])[CH:12]=[CH:13][CH:14]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.CC1(C)N([O])C(C)(C)CCC1.C(O)(=O)C.C(O)(=O)C.IC1C=CC=CC=1>>[CH2:1]([O:8][C:9]1[CH:10]=[C:11]([C:15](=[O:19])/[CH:16]=[CH:17]/[CH3:18])[CH:12]=[CH:13][CH:14]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1Participants
4
Procedure
93.C was prepared from 93.B via oxidation with TEMPO and iodobenzene diacetate according to the analogous method described in Example 90.
Sources & evidence
- ORD record
- ord-01771bad06914b56804b1e2a58b95f0d
- Source dataset
- uspto-grants-2011_10
- Patent number
- US08030354B2
Reaction notes
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