Potassium Chloride → POTASSIUM TETRAPHENYLBORATE 97

HRID 1089097Notes

Reaction equation

HRID 1089097 reaction equation
[C:1]1([B-:7]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Na+].[Cl-].[K+:28].[K].C1([B-](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>O>[C:20]1([B-:7]([C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)([C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=2)[C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=1.[K+:28]

Participants

6

Procedure

A solution was prepared by dissolving 10.27 grams (0.30 moles) of Aldrich sodiumtetraphenylborate in 250 milliliters of distilled water. To this, while stirring, was added a solution of 2.36 grams (0.32 moles) of Fisher reagent grade potassium chloride dissolved in 100 milliliters of distilled water. The white precipitate that formed was stirred for 10 minutes and filtered. The precipitate was then washed with distilled water and filtered, followed by drying at 60° C. under vacuum for 24 hours. Total yield was 10.20 grams (0.28 moles) of the potassium salt of tetraphenylborate.

Workup

  1. customA solution was prepared
  2. customThe white precipitate that formed
  3. stirringwas stirred for 10 minutes
  4. filtrationfiltered
  5. washThe precipitate was then washed with distilled water
  6. filtrationfiltered
  7. customby drying at 60° C. under vacuum for 24 hours

Sources & evidence

ORD record
ord-2c5193e4e00c484e9b291018426e10f5
Source dataset
uspto-grants-1990_10
Patent number
US04965158

Reaction notes

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