Pyridine → Borate(1-), tetrafluoro-, hydrogen, compd. with pyridine (1:1:1)

HRID 2040734

Reaction equation

HRID 2040734 reaction equation
[F:1][B-:2]([F:5])([F:4])[F:3].[H+].[N:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1>>[F:1][B-:2]([F:5])([F:4])[F:3].[NH+:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1

Participants

3

Procedure

Tetrafluoroboric acid (250 ml, 2.00 mol) was added to cool (0° C.) pyridine (157.7 ml, 1.95 mol) within 25 mins. resulting in a colorless precipitate. After the acid was completely added, the mixture was further stirred for 30 mins. and held at the same temperature. Thereafter, the reaction mixture was filtered. The residue was washed twice with cold ethanol and dried for 12 hrs at high vacuum to yield 201.9 g (60%) of pyridiniumtetrafluoroborate in the form of colorless crystals.

Workup

  1. customresulting in a colorless precipitate
  2. additionAfter the acid was completely added
  3. filtrationThereafter, the reaction mixture was filtered
  4. washThe residue was washed twice with cold ethanol
  5. customdried for 12 hrs at high vacuum

Sources & evidence

ORD record
ord-f5fcc54c85f841f4aa5b5eefbfc31644
Source dataset
uspto-grants-2013_11
Patent number
US08580949B2

Linked notes

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