Trifluoroacetic acid → Trifluoroacetic acid
Reaction equation
C(OC(=O)[NH:7][CH2:8][CH2:9][C:10](=[O:13])[NH:11][CH3:12])(C)(C)C.[F:15][C:16]([F:21])([F:20])[C:17]([OH:19])=[O:18]>ClCCl>[NH2:7][CH2:8][CH2:9][C:10]([NH:11][CH3:12])=[O:13].[C:17]([OH:19])([C:16]([F:21])([F:20])[F:15])=[O:18]Participants
5
Reactant 2
Product 2
Reagents, catalysts & solvents 1
Procedure
(2-Methylcarbamoyl-ethyl)-carbamic acid tert-butyl ester (534 mg, 2.64 mmol) was dissolved in dichloromethane (10 mL) and the solution was treated with trifluoroacetic acid (3 mL). The reaction was allowed to stir overnight at room temperature. The solvent and excess TFA was then concentrated to afford 3-Amino-N-methyl-propionamide as a crude TFA salt. The crude material (270 mg) was used without further purification.
Workup
- concentrationThe solvent and excess TFA was then concentrated
Sources & evidence
- ORD record
- ord-7c228b50352c4dc79a47aea0d73b95f3
- Source dataset
- uspto-grants-2013_10
- Patent number
- US08552186B2
Reaction notes
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