Ethyl Acetoacetate → HCID 13299634, compound
Reaction equation
[CH2:1]([CH:4]([C:10](=[O:12])[CH3:11])[C:5]([O:7][CH2:8][CH3:9])=[O:6])[CH:2]=[CH2:3].C(OCC)(=O)CC(C)=O>>[CH2:1]([CH:4]([CH:10]([OH:12])[CH3:11])[C:5]([O:7][CH2:8][CH3:9])=[O:6])[CH:2]=[CH2:3]Participants
3
Procedure
Ethyl 2-allyl-3-hydroxybutyrate was prepared following the procedure as described in step 1) of Preparation Example 2, except for that ethyl 2-allyl-3-oxo-butyrate was used to replace for ethyl acetoacetate. Yield 60%.
Workup
- customof Preparation Example 2
Sources & evidence
- ORD record
- ord-fdae658a95df45c699bb4d2322dff131
- Source dataset
- uspto-grants-2008_04
- Patent number
- US07351778B2
Reaction notes
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