Sodium Hydroxide → 5,5,5-Trifluoro-3-(2,2,2-trifluoroethyl)-DL-norvaline
Reaction equation
[F:1][C:2]([F:18])([F:17])[CH2:3][CH:4]([CH:10]1[NH:14]C(=O)N[C:11]1=[O:16])[CH2:5][C:6]([F:9])([F:8])[F:7].[OH-:19].[Na+]>>[F:1][C:2]([F:18])([F:17])[CH2:3][CH:4]([CH2:5][C:6]([F:9])([F:8])[F:7])[CH:10]([C:11]([OH:19])=[O:16])[NH2:14]Participants
3
Procedure
5-(3,3,3-Trifluoro-1-(2,2,2-trifluoroethyl)propyl) imidazolidine-2,4-dione (1.0 g, 3.59 mmol) was dissolved in a 10 mL solution of aqueous NaOH (0.575 g in 10 mL H2O, 14.38 mmol). The solution was divided in 2 special vessels for microwave technology. The solution was heated by microwave in sealed vessels for 1 h. Microwave conditions: 15 min at about 100% power, 150° C., 50 psi, then 5 min at rest, 0% power. The sequence was repeated until the reaction was done. Water and ammonia were removed from the reaction mixture in vacuo and the resulting crude 5,5,5-trifluoro-3-(2,2,2-trifluoroethyl)-dl-norvaline (0.92 g, 100%) and NaOH mixture was used in the next reaction without further purification.
Workup
- temperatureThe solution was heated by microwave in sealed vessels for 1 h
- custom15 min
- customat about 100% power, 150° C., 50 psi
- custom5 min
- customWater and ammonia were removed from the reaction mixture in vacuo
- customthe resulting crude 5,5,5-trifluoro-3-(2,2,2-trifluoroethyl)-dl-norvaline (0.92 g, 100%) and NaOH mixture was used in the next reaction without further purification
Sources & evidence
- ORD record
- ord-8c420ec88e4142e4a5714dfed681779d
- Source dataset
- uspto-grants-2007_11
- Patent number
- US07300951B2
Reaction notes
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