Perchloric Acid → 1-Boc-3-aminopyrrolidine
Reaction equation
Cl(O)(=O)(=O)=O.[C:6]([O:10][C:11]([N:13]1[CH2:17][CH2:16][C@H:15]([NH2:18])[CH2:14]1)=[O:12])([CH3:9])([CH3:8])[CH3:7].C(OC(N1CC[C@@H](N)C1)=O)(C)(C)C>>[C:6]([O:10][C:11]([N:13]1[CH2:17][CH2:16][CH:15]([NH2:18])[CH2:14]1)=[O:12])([CH3:9])([CH3:7])[CH3:8]Participants
4
Procedure
column: manufactured by Daicel Chemical Industries, Ltd., {CROWNPAK 150×4.6 mm}, mobile phase: aqueous perchloric acid solution (pH 1.5), flow rate: 1.0 ml/min, detection: UV 210 nm, column temperature: 35° C., retention time: (S)-1-(tert-butoxycarbonyl)-3-aminopyrrolidine; 24.1 min, (R)-1-(tert-butoxycarbonyl)-3-aminopyrrolidine; 27.0 min
Workup
- custom35° C., retention time
- custom27.0 min
Sources & evidence
- ORD record
- ord-f0c34cbfd1eb41c8a015092b4636d72c
- Source dataset
- uspto-grants-2011_10
- Patent number
- US08030501B2
Reaction notes
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