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Sodium Tetrafluoroborate → 4-Aza-1-azoniabicyclo[2.2.2]octane, 1-(chloromethyl)-, tetrafluoroborate(1-) (1:1)

HRID 1534079
Notes
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Reaction equation

HRID 1534079 reaction equation
[F:1][B-:2]([F:5])([F:4])[F:3].[Na+].[Cl-].[Cl:8][CH2:9][N+:10]12[CH2:17][CH2:16][N:13]([CH2:14][CH2:15]1)[CH2:12][CH2:11]2>C(#N)C>[F:1][B-:2]([F:5])([F:4])[F:3].[Cl:8][CH2:9][N+:10]12[CH2:17][CH2:16][N:13]([CH2:14][CH2:15]1)[CH2:12][CH2:11]2
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 4343483Sodium TetrafluoroborateHCID 109979444-Aza-1-azoniabicyclo(2.2.2)octane, 1-(chloromethyl)-, chloride (1:1)

Product 1

HCID 152521384-Aza-1-azoniabicyclo[2.2.2]octane, 1-(chloromethyl)-, tetrafluoroborate(1-) (1:1)Yield 84.4%

Reagents, catalysts & solvents 1

HCID 6342AcetonitrileSolvent

Procedure

Sodium tetrafluoroborate (1.97 g, 17.9 mmol) in dry acetonitrile (20 cm3) was run slowly into a stirred slurry of 1-chloromethyl-4-aza-1-azoniabicyclo[2,2,2]-octane chloride (3.53 g, 17.9 mmol) (a known compound, see B. Almarzogi et al., Tetrahedron, 1986, 42, 601) in the same solvent (20 cm3) at ambient temperature under an atmosphere of dry nitrogen. After being stirred overnight, the reaction mixture was filtered to remove lithium chloride which had precipitated. The precipitate was washed with dry acetonitrile (20 cm3) and the washings plus the filtrate were evaporated to provide slightly impure (according to n.m.r. analysis) and very pale yellow 1-chloromethyl-4-aza-1-azoniabicyclo [2.2.2]octane tetrafluoroborate (3.75 g, 15.1 mmol, 84%) [δF (solution in D2O; ext. CF3CO2H ref.) -74.3 (s; BF4-) p.p.m., δH (same soln.) 3.29 (m; 3×CH2), 3.57 (m; 3 ×CH2), 5.11 (s; CH2Cl) p.p.m. (residual H in D2O, 4.75 p.p.m.)]. Recrystallisation of a small quantity of this product from an ethanol-diethyl ether mixture gave a pure white sample, m.p. 152° C., which appeared to be non-hygroscopic.

Workup

  1. customat ambient temperature
  2. filtrationthe reaction mixture was filtered
  3. customto remove lithium chloride which
  4. customhad precipitated
  5. washThe precipitate was washed with dry acetonitrile (20 cm3)
  6. customthe washings plus the filtrate were evaporated

Sources & evidence

ORD record
ord-22abf1e1e1bf43c0aaf469ae03a30697
Source dataset
uspto-grants-1992_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05086178

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes