Hydrochloric Acid → 2-Amino-4,4,4-trifluorobutanamide hydrochloride
Reaction equation
[NH2:1][C:2](=[O:17])[CH:3]([NH:9]C(=O)OC(C)(C)C)[CH2:4][C:5]([F:8])([F:7])[F:6].[ClH:18]>O1CCOCC1>[ClH:18].[NH2:9][CH:3]([CH2:4][C:5]([F:8])([F:7])[F:6])[C:2]([NH2:1])=[O:17]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of the solid tert-butyl 1-amino-4,4,4-trifluoro-1-oxobutan-2-ylcarbamate in dioxane (4 mL) and aq. 6N HCl (6 mL) was stirred at room temperature for 1 h. It was then concentrated in vacuo to give 2-amino-4,4,4-trifluorobutanamide hydrochloride as a solid (135 mg).
Workup
- concentrationIt was then concentrated in vacuo
Sources & evidence
- ORD record
- ord-8cee082e5e834c4b916c5319656b98d9
- Source dataset
- uspto-grants-2014_09
- Patent number
- US08846928B2
Reaction notes
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