Catecholborane → trans-3-Methyl-3-(4-trifluoromethylphenyl)-1-butenylboronic acid

HRID 1939700Notes

Reaction equation

HRID 1939700 reaction equation
[CH3:1][C:2]([C:6]1[CH:11]=[CH:10][C:9]([C:12]([F:15])([F:14])[F:13])=[CH:8][CH:7]=1)([CH3:5])[C:3]#[CH:4].[O:16]1C2C=CC=CC=2[O:18][BH:17]1>>[CH3:5][C:2]([C:6]1[CH:11]=[CH:10][C:9]([C:12]([F:14])([F:13])[F:15])=[CH:8][CH:7]=1)([CH3:1])/[CH:3]=[CH:4]/[B:17]([OH:18])[OH:16]

Participants

3

Conditions

Temperature
70 °C

Procedure

Under a nitrogen atmosphere, a stirred mixture of 25.2 grams (0.12 mole) of 3-methyl-3-(4-trifluoromethylphenyl)-1-butyne and 12.7 mL (0.12 mole) of 1,3,2-benzodioxaborole was warmed to 70° C. where it stirred for six hours. The reaction mixture was then cooled and poured slowly into 500 mL of ice-water while flushing with nitrogen. The mixture was then allowed to warm to ambient temperature where it stirred for about 18 hours. The mixture was cooled in an ice-bath, and the resultant solid was collected by filtration. The solid was washed with water and then dissolved in diethyl ether. The solution was washed with 100 mL of an aqueous solution saturated with sodium chloride. The organic layer was dried with magnesium sulfate, filtered, and concentrated under reduced pressure to a residual solid. The solid was dried under vacuum without heat, yielding 27.6 grams of trans-3-methyl-3-(4-trifluoromethylphenyl)-1-butenylboronic acid.

Workup

  1. temperatureThe reaction mixture was then cooled
  2. customwhile flushing with nitrogen
  3. temperatureto warm to ambient temperature where it
  4. stirringstirred for about 18 hours
  5. temperatureThe mixture was cooled in an ice-bath
  6. filtrationthe resultant solid was collected by filtration
  7. washThe solid was washed with water
  8. dissolutiondissolved in diethyl ether
  9. washThe solution was washed with 100 mL of an aqueous solution saturated with sodium chloride
  10. dry with materialThe organic layer was dried with magnesium sulfate
  11. filtrationfiltered
  12. concentrationconcentrated under reduced pressure to a residual solid
  13. customThe solid was dried under vacuum
  14. temperaturewithout heat

Sources & evidence

ORD record
ord-e62ba3f2c8db46dfb08ab3cec5cf0d0d
Source dataset
uspto-grants-1997_12
Patent number
US05696259

Reaction notes

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