Hydrochloric Acid → HCID 18734737, compound
Reaction equation
[N:1]([CH2:4][C@H:5]([NH:11]C(OC(C)(C)C)=O)[C:6]([O:8][CH2:9][CH3:10])=[O:7])=[N+:2]=[N-:3].[ClH:19]>C(OCC)(=O)C>[ClH:19].[NH2:11][C@@H:5]([CH2:4][N:1]=[N+:2]=[N-:3])[C:6]([O:8][CH2:9][CH3:10])=[O:7]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of ethyl 3-azido-2(S)-(tert-butoxycarbonylamino)propionate (0.5 g) in ethyl acetate (5 ml) was added 4N HCl in ethyl acetate (5 ml) at 0° C. After stirring at room temperature for 2 hours, the mixture was evaporated in vacuo. The residue was recrystallized from diethyl ether to give ethyl 2(S)-amino-3-azidopropionate hydrochloride (0.3 g).
Workup
- customthe mixture was evaporated in vacuo
- customThe residue was recrystallized from diethyl ether
Sources & evidence
- ORD record
- ord-e0de9e0b5c4d4cb180f536711c718717
- Source dataset
- uspto-grants-2002_04
- Patent number
- US06380215B1
Reaction notes
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