Water → p-Methylphenoxyacetic acid

HRID 1710219Notes

Reaction equation

HRID 1710219 reaction equation
[H-].[Na+].[CH3:3][C:4]1[CH:9]=[CH:8][C:7]([OH:10])=[CH:6][CH:5]=1.Cl[CH2:12][C:13]([O-:15])=[O:14].[Na+].O>CCCCCC.C1COCC1.CS(C)=O>[CH3:3][C:4]1[CH:9]=[CH:8][C:7]([O:10][CH2:12][C:13]([OH:15])=[O:14])=[CH:6][CH:5]=1

Participants

8

Conditions

Temperature
-15 °C

Procedure

Sodium hydride (0.86 g of 60% NaH in oil=0.516 g, 21.5 mmol) in oil dispersion was washed twice with 10 ml of hexane. THF was added (5 ml) and the mixture was cooled to -15° C. A solution of p-methylphenol (1.95 g, 18 mmol) in THF was then added, and the mixture was warmed to 25° C. for 1 hour. The THF was removed by distillation under vacuum and a solution of sodium chloroacetate (2.5 g, 22 mmol) in DMSO (50 ml) was added. The mixture was stirred at room temperature for 20 hours, then diluted with 300 ml. of water. The mixture was extracted twice with 50 ml. of hexane. The aqueous phase was acidified with 4N hydrochloric acid and the product was extracted twice with 100 ml. of ethyl acetate. The combined ethyl acetate layers were washed twice with 100 ml. water, dried over MgSO4, filtered, and the solvent was removed by distillation under reduced pressure to give 2.9 g of product as a white solid. Yield of product=97.6%.

Workup

  1. temperaturethe mixture was warmed to 25° C. for 1 hour
  2. customThe THF was removed by distillation under vacuum
  3. additiondiluted with 300 ml
  4. extractionThe mixture was extracted twice with 50 ml
  5. extractionthe product was extracted twice with 100 ml
  6. washThe combined ethyl acetate layers were washed twice with 100 ml
  7. dry with materialwater, dried over MgSO4
  8. filtrationfiltered
  9. customthe solvent was removed by distillation under reduced pressure

Sources & evidence

ORD record
ord-bf222f4c0904409197435117376d00a7
Source dataset
uspto-grants-1990_08
Patent number
US04952724

Reaction notes

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