Hydrochloric Acid → 2-(2-Methylphenoxy)acetic acid

HRID 1429436Notes

Reaction equation

HRID 1429436 reaction equation
[C:1]1([CH3:8])[C:6]([OH:7])=[CH:5][CH:4]=[CH:3][CH:2]=1.Br[CH2:10][C:11]([O:13]CC)=[O:12].C([O-])([O-])=O.[K+].[K+].[OH-].[Na+].Cl>CC#N.O.CCO>[C:1]1([CH3:8])[CH:2]=[CH:3][CH:4]=[CH:5][C:6]=1[O:7][CH2:10][C:11]([OH:13])=[O:12]

Participants

8

Conditions

Temperature
80 °C

Procedure

To a stirred solution of o-cresol (200 mg, 1.85 mmol) in MeCN (5 mL) was added ethyl bromoacetate (461 mg, 2.78 mmol) and K2CO3 (766 mg, 5.55 mmol). The mixture was stirred at 80° C. for 4 hours. The mixture was filtered and the filtrate concentrated. NaOH (150 mg, 3.70 mmol) and H2O/EtOH (1:1, 10 mL) was then added to the mixture and the mixture stirred at 50° C. for 4 hours. After cooling, the mixture was acidified by adding 1M HCl then extracted with ethyl acetate (2×30 mL). The combined organic extracts were washed with brine (30 mL), dried over anhydrous Na2SO4 and concentrated. The residue was used directly in the next step without further purification.

Workup

  1. filtrationThe mixture was filtered
  2. concentrationthe filtrate concentrated
  3. stirringthe mixture stirred at 50° C. for 4 hours
  4. temperatureAfter cooling
  5. extractionthen extracted with ethyl acetate (2×30 mL)
  6. washThe combined organic extracts were washed with brine (30 mL)
  7. dry with materialdried over anhydrous Na2SO4
  8. concentrationconcentrated
  9. customThe residue was used directly in the next step without further purification

Sources & evidence

ORD record
ord-a8a9a251a0884aa0909c761aef199ba0
Source dataset
uspto-grants-2015_01
Patent number
US08940726B2

Reaction notes

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