Hydrochloric Acid → Methyl 3-amino-4,4,4-trifluorobutanoate--hydrogen chloride (1/1)
Reaction equation
[NH2:1][CH:2]([C:7]([F:10])([F:9])[F:8])[CH2:3][C:4]([OH:6])=[O:5].[ClH:11].[CH3:12]O>>[ClH:11].[NH2:1][CH:2]([C:7]([F:10])([F:9])[F:8])[CH2:3][C:4]([O:6][CH3:12])=[O:5]Participants
4
Procedure
1.5 g of 3-amino-4,4,4-trifluorobutanoic acid (9.55 mmol, 1 equivalent) were initially charged in 18 ml of methanol which had been saturated with hydrogen chloride, and the mixture was stirred under reflux for 4 h. The reaction solution was then concentrated, evaporated repeatedly with dichloromethane and dried under reduced pressure. This gave 1.86 g (94% of theory) of the title compound.
Workup
- temperatureunder reflux for 4 h
- concentrationThe reaction solution was then concentrated
- customevaporated repeatedly with dichloromethane
- customdried under reduced pressure
Sources & evidence
- ORD record
- ord-2af68bb6432f48898e02e28e98046c54
- Source dataset
- uspto-grants-2014_08
- Patent number
- US08796305B2
Reaction notes
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