Potassium Hydroxide → 2-(4-Bromophenyl)-2-methylpropanoic acid

HRID 2078126Notes

Reaction equation

HRID 2078126 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([CH3:14])([CH3:13])[C:9]([O:11]C)=[O:10])=[CH:4][CH:3]=1.[OH-].[K+]>CCO.O>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]([CH3:14])([CH3:13])[C:9]([OH:11])=[O:10])=[CH:6][CH:7]=1

Participants

5

Conditions

Temperature
90 °C

Procedure

A solution of methyl 2-(4-bromophenyl)-2,2-dimethylacetate (3880 μL, 15090 μmol) in EtOH (80 mL) and water (20 mL) was treated with KOH (4233 mg, 75450 μmol). The reaction was heated to 90° C. After 15 hours, the reaction was cooled to 23° C. and concentrated in vacuo. The crude mixture was partitioned between water/diethyl ether (150 mL each). The aqueous layer was separated and extracted with diethyl ether (100 mL). The combined ether layers were then extracted with a 1N NaOH solution (25 mL). The combined aqueous washes were acidified with concentrated HCl to pH=2.0 and extracted with EtOAc (3×100 mL). The combined EtOAc layers were dried over MgSO4, and concentrated in vacuo to afford 3144 mg of 2-(4-bromophenyl)-2-methylpropanoic acid.

Workup

  1. temperaturethe reaction was cooled to 23° C.
  2. concentrationconcentrated in vacuo
  3. customThe crude mixture was partitioned between water/diethyl ether (150 mL each)
  4. customThe aqueous layer was separated
  5. extractionextracted with diethyl ether (100 mL)
  6. extractionThe combined ether layers were then extracted with a 1N NaOH solution (25 mL)
  7. extractionextracted with EtOAc (3×100 mL)
  8. dry with materialThe combined EtOAc layers were dried over MgSO4
  9. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-443b1dc86faa449eadd37735b59b2d84
Source dataset
uspto-grants-2011_04
Patent number
US07928139B2

Reaction notes

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