Reaction equation
C[O:2][C:3]1[CH:4]=[C:5]([CH:11]=[CH:12][C:13]([C:15]2[CH:20]=[CH:19][CH:18]=[C:17]([OH:21])[CH:16]=2)=[O:14])[CH:6]=[CH:7][C:8]=1[O:9][CH3:10].C1C(C=O)=CC2OCOC=2C=1>>[OH:21][C:17]1[CH:16]=[C:15]([CH:20]=[CH:19][CH:18]=1)[C:13](=[O:14])[CH:12]=[CH:11][C:5]1[CH:6]=[CH:7][C:8]2[O:9][CH2:10][O:2][C:3]=2[CH:4]=1Participants
3
Procedure
Prepared in a similar manner as (4) from piperonal. Crude solids (26.7 g, 100%) were carried on directly to the next reaction step without chromatographic purification or characterization.
Workup
- customdirectly to the next reaction step
- customwithout chromatographic purification or characterization
Sources & evidence
- ORD record
- ord-46dc9efd0b5940438acf900e5592d988
- Source dataset
- uspto-grants-2012_01
- Patent number
- US08106191B2
Linked notes
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