Dichloromethane → HCID 23087516, compound
Reaction equation
C([O:5][C:6](=O)[N:7]([CH2:9][CH2:10][O:11][CH2:12][CH3:13])[CH3:8])(C)(C)C.FC(F)(F)C(O)=O.[Cl:22][CH2:23]Cl>>[Cl:22][CH2:23][C:6]([N:7]([CH2:9][CH2:10][O:11][CH2:12][CH3:13])[CH3:8])=[O:5]Participants
4
Procedure
To a solution of tert-butyl(2-ethoxyethyl)methylcarbamate (1.2 g) in dichloromethane (6 ml) was added trifluoroacetic acid (6 ml) on an ice bath. The solution was stirred for 30 minutes while warming to room temperature, then the solvent was evaporated in vacuo. Synthesized from the resulting (2-ethoxyethyl)methylamine trifluoroacetate (crude product) (2.3 g) according to an analogous synthetic method to Preparation Example 119, the title compound (799 mg) was obtained.
Workup
- customthe solvent was evaporated in vacuo
- customSynthesized from the resulting (2-ethoxyethyl)methylamine trifluoroacetate (crude product) (2.3 g)
- customaccording to an analogous synthetic method to Preparation Example 119
Sources & evidence
- ORD record
- ord-78cf3caa451f48f98973d9d431c76c92
- Source dataset
- uspto-grants-2009_11
- Patent number
- US07612114B2
Reaction notes
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