Sodium Hydroxide → p-Methylphenoxyacetic acid

HRID 1777100Notes

Reaction equation

HRID 1777100 reaction equation
[C:1]1([CH3:14])[CH:6]=[CH:5][C:4]([O:7][CH2:8][C:9]([O:11]CC)=[O:10])=[CH:3][CH:2]=1.[OH-].[Na+]>CCO>[C:1]1([CH3:14])[CH:6]=[CH:5][C:4]([O:7][CH2:8][C:9]([OH:11])=[O:10])=[CH:3][CH:2]=1

Participants

4

Procedure

To a solution of ethyl 2-(p-tolyloxy)acetate (200 mg, 1 mmol) in EtOH (10 ml) was added 10% NaOH solution (10 ml) at 26° C. The mixture was stirred for 30 min, concentrated then water (20 mL) added to it before washing with ethyl acetate (2×20 mL). The aqueous layer was acidified with 2N HCL until pH 3 and extracted with EA (2×20 ml). The organic layer was washed with brine (30 mL), dried over Na2SO4 and concentrated to give the title compound which was used in next step without further purification.

Workup

  1. concentrationconcentrated
  2. additionwater (20 mL) added to it
  3. washbefore washing with ethyl acetate (2×20 mL)
  4. extractionextracted with EA (2×20 ml)
  5. washThe organic layer was washed with brine (30 mL)
  6. dry with materialdried over Na2SO4
  7. concentrationconcentrated

Sources & evidence

ORD record
ord-32e06f896d6b4a05bef987b40a21f46d
Source dataset
uspto-grants-2016_02
Patent number
US09266836B2

Reaction notes

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