Ammonium Acetate → HCID 66924664, compound
Reaction equation
[C:1]([CH:4]([CH:10](C)[C:11](=O)[C:12]1[CH:16]=[CH:15][S:14][CH:13]=1)[C:5]([O:7][CH2:8][CH3:9])=[O:6])(=O)[CH3:2].C([O-])(=O)C.[NH4+:23]>>[CH3:2][C:1]1[NH:23][C:11]([C:12]2[CH:16]=[CH:15][S:14][CH:13]=2)=[CH:10][C:4]=1[C:5]([O:7][CH2:8][CH3:9])=[O:6]Participants
3
Procedure
Using ethyl 2-acetyl-3-methyl-4-oxo-4-(3-thienyl)butanoate (1.86 g) and ammonium acetate (626 mg), a procedure as in Reference Example 14 was performed to give the title compound as a brown oil (yield 1.57 g, 91%).
Sources & evidence
- ORD record
- ord-ffa2e79740bb4803b23ad0b06a460de7
- Source dataset
- uspto-grants-2011_11
- Patent number
- US08048909B2
Reaction notes
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