Hydrochloric Acid → 2-(2-Methylphenoxy)acetic acid
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
- filtrationThe mixture was filtered
- concentrationthe filtrate concentrated
- stirringthe mixture stirred at 50° C. for 4 hours
- temperatureAfter cooling
- extractionthen extracted with ethyl acetate (2×30 mL)
- washThe combined organic extracts were washed with brine (30 mL)
- dry with materialdried over anhydrous Na2SO4
- concentrationconcentrated
- 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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