Water → Ethyl 2-methylbiphenyl-4-carboxylate

HRID 731926Notes

Reaction equation

HRID 731926 reaction equation
O.C(=O)([O-])[O-].[Na+].[Na+].[C:8]1(B(O)O)[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.Br[C:18]1[CH:28]=[CH:27][C:21]([C:22]([O:24][CH2:25][CH3:26])=[O:23])=[CH:20][C:19]=1[CH3:29]>C1(C)C=CC=CC=1>[CH3:29][C:19]1[CH:20]=[C:21]([C:22]([O:24][CH2:25][CH3:26])=[O:23])[CH:27]=[CH:28][C:18]=1[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1

Participants

6

Procedure

Into 150 ml of water were suspended 55.9 g of sodium carbonate and 38.6 g of phenylboronic acid. Thereto was added 51.4 g of ethyl 4-bromo-3-methylbenzoate dissolved in 400 ml of toluene and then was added 4.0 g of tetrakistriphenylphosphine palladium, followed by 2 hours of reflux with heating. After the reaction solution was cooled to room temperature, filtration was conducted using celite, water was added to the filtrate and the organic layer was extracted with toluene. After the organic layer was dried over anhydrous magnesium sulfate, the solvent was removed by evaporation and the resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate) to obtain 50.4 g of ethyl 2-methylbiphenyl-4-carboxylate as a colorless oil.

Workup

  1. temperatureof reflux
  2. temperaturewith heating
  3. filtrationfiltration
  4. additionwas added to the filtrate
  5. extractionthe organic layer was extracted with toluene
  6. dry with materialAfter the organic layer was dried over anhydrous magnesium sulfate
  7. customthe solvent was removed by evaporation
  8. customthe resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate)

Sources & evidence

ORD record
ord-dafac2bafbb7438cb180c083188183a2
Source dataset
uspto-grants-2009_09
Patent number
US07585878B2

Reaction notes

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