Tetrafluoroboric acid → 1-Methylpyrrolidine
Reaction equation
COC(=O)[O-].[CH3:6][N+:7]1(C)[CH2:11][CH2:10][CH2:9][CH2:8]1.[H+].[B-:14]([F:18])([F:17])([F:16])[F:15]>>[CH3:6][N:7]1[CH2:11][CH2:10][CH2:9][CH2:8]1.[F:15][B-:14]([F:18])([F:17])[F:16]Participants
4
Procedure
By following the same procedure (2nd step) of Example 1 except that 10.0 g of N,N-dimethylpyrrolidinium methyl carbonate thus obtained and 12.9 g of an aqueous solution of 42% HBF4 were used, 10.1 g (yield of 92.4% to N-methylpyrrolidine) of high-pure dimthylpyrrolidinium tetrafluoroborate was obtained.
Workup
- customthus obtained
Sources & evidence
- ORD record
- ord-c32bd56736a34e96833fff603be0fc05
- Source dataset
- uspto-grants-1990_01
- Patent number
- US04892944
Reaction notes
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