Triethylamine → Acetic Anhydride
Reaction equation
CS(O)(=O)=[O:3].[NH2:6][C@H:7]([CH3:13])[CH2:8][C:9]([O:11][CH3:12])=[O:10].C(N([CH2:19][CH3:20])CC)C>>[C:19]([NH:6][C@H:7]([CH3:13])[CH2:8][C:9]([O:11][CH3:12])=[O:10])(=[O:3])[CH3:20].[C:9]([O:11][C:19](=[O:3])[CH3:20])(=[O:10])[CH3:8]Participants
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Procedure
The enantiomeric excess was measured after conversion of the methyl (R)-3-aminobutanoate methanesulfonate obtained into methyl (R)-3-acetamidobutanoate by acetylation with acetic anhydride in the presence of triethylamine, and was found to be 85.0% ee.
Sources & evidence
- ORD record
- ord-e885c55923e7492ab7d94c7446f67166
- Source dataset
- uspto-grants-2011_02
- Patent number
- US07893296B2
Reaction notes
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