p-Toluenesulfonic acid → Ethyl 2-(4-phenoxyphenyl)acetate

HRID 1249679Notes

Reaction equation

HRID 1249679 reaction equation
[O:1]([C:8]1[CH:13]=[CH:12][C:11]([CH2:14][C:15]([O-:17])=[O:16])=[CH:10][CH:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:18]1(C)C=CC(S(O)(=O)=O)=C[CH:19]=1>C(O)C>[O:1]([C:8]1[CH:9]=[CH:10][C:11]([CH2:14][C:15]([O:17][CH2:18][CH3:19])=[O:16])=[CH:12][CH:13]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

4

Reactant 2

HCID 6101p-Toluenesulfonic acidHCID 20392587(4'-Phenoxyphenyl)acetate

Product 1

HCID 13567666Ethyl 2-(4-phenoxyphenyl)acetateYield 404.9%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

To a suspension of (4′-phenoxyphenyl)acetate acid (0.456 g) in 4 ml of ethanol is added para-toluensulfonic acid (0.076 g) and the resulting mixture is refluxed for 2 hours. The solvent is evaporated off, the residue is dissolved in diethyl ether and the organic phase is washed with saturated aqueous solution of sodium hydrogencarbonate and then with brine. The organic phase is dried over sodium sulfate and concentrated to dryness to give 0.458 g of the product as a brown oil.

Workup

  1. temperaturethe resulting mixture is refluxed for 2 hours
  2. customThe solvent is evaporated off
  3. dissolutionthe residue is dissolved in diethyl ether
  4. washthe organic phase is washed with saturated aqueous solution of sodium hydrogencarbonate
  5. dry with materialThe organic phase is dried over sodium sulfate
  6. concentrationconcentrated to dryness

Sources & evidence

ORD record
ord-e3792e93bf5d4c318046ce40ccaad68a
Source dataset
uspto-grants-2002_01
Patent number
US06335332B1

Reaction notes

Loading…