Trifluoroacetic acid → HCID 86744971, compound
Reaction equation
[CH3:1][O:2][C:3](=[O:20])[CH2:4][NH:5][C:6](=[O:19])[C@H:7]([CH:16]([CH3:18])[CH3:17])[NH:8]C(OC(C)(C)C)=O.[F:21][C:22]([F:27])([F:26])[C:23]([OH:25])=[O:24]>>[F:21][C:22]([F:27])([F:26])[C:23]([OH:25])=[O:24].[CH3:1][O:2][C:3](=[O:20])[CH2:4][NH:5][C:6](=[O:19])[C@H:7]([CH:16]([CH3:17])[CH3:18])[NH2:8]Participants
3
Procedure
t-butyloxycarbonyl-L-valyl-glycine methyl ester (1.44 g, 5 mmol) was dissolved in trifluoroacetic acid (5 ml), and the mixture was left at room temperature for 1 hour. The solution was evaporated to dryness in vacuo and the residue triturated with dry ether.
Workup
- customThe solution was evaporated to dryness in vacuo
- customthe residue triturated with dry ether
Sources & evidence
- ORD record
- ord-79272b99fddf470bb0548622df5394de
- Source dataset
- uspto-grants-1991_08
- Patent number
- US05037957
Reaction notes
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