Trifluoroacetic acid → 181495-37-4
Reaction equation
[CH2:1]([O:8][CH2:9][C@H:10]([NH:12]C(OC(C)(C)C)=O)[CH3:11])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.FC(F)(F)C(O)=O>C(Cl)Cl>[CH2:1]([O:8][CH2:9][C@H:10]([NH2:12])[CH3:11])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 0 °C
Procedure
Dissolve (R)-3-benzyloxy-2-(tert-butoxycarbonylamino)-propane (800 mg, 3 mmol) in DCM (10 mL), add trifluoroacetic acid (5 mL), and stir at 0° C. for 20 min. Evaporate and purify by SCX chromatography to give the title compound as a colorless oil (440 mg, 89%). MS (ES+) m/z: 166 (M+H)+.
Workup
- customEvaporate
- custompurify by SCX chromatography
Sources & evidence
- ORD record
- ord-05188244d3c44fbba9d7d4d7656c25fd
- Source dataset
- uspto-grants-2011_09
- Patent number
- US08022062B2
Reaction notes
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