Trifluoroacetic acid → 3-(Trifluoromethyl)pyrrolidine (trifluoroacetate)
Reaction equation
[F:1][C:2]([F:16])([F:15])[CH:3]1[CH2:7][CH2:6][N:5](C(OC(C)(C)C)=O)[CH2:4]1.[C:17]([C:21]([OH:23])=[O:22])([F:20])([F:19])[F:18]>C(Cl)Cl>[F:18][C:17]([F:20])([F:19])[C:21]([OH:23])=[O:22].[F:1][C:2]([F:16])([F:15])[CH:3]1[CH2:7][CH2:6][NH:5][CH2:4]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
tert-Butyl 3-(trifluoromethyl)pyrrolidine-1-carboxylate (100 mg, 0.42 mmol) was treated with 20% CF3CO2H in CH2Cl2 at room temperature overnight. The volatiles were removed in vacuo to give the subtitled compound (106 mg).
Workup
- customThe volatiles were removed in vacuo
Sources & evidence
- ORD record
- ord-7f428b61f37541c99339f78fcbc55949
- Source dataset
- uspto-grants-2008_11
- Patent number
- US07449475B2
Reaction notes
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