Citric Acid → Methyl 4-bromo-α,α-dimethylbenzenepropanoate

HRID 1384252Notes

Reaction equation

HRID 1384252 reaction equation
C([Li])CCC.C(NC(C)C)(C)C.[C:13]([O:18][CH3:19])(=[O:17])[CH:14]([CH3:16])[CH3:15].[Br:20][C:21]1[CH:28]=[CH:27][C:24]([CH2:25]Br)=[CH:23][CH:22]=1.C(O)(=O)CC(CC(O)=O)(C(O)=O)O>CCCCCC.O1CCCC1>[Br:20][C:21]1[CH:28]=[CH:27][C:24]([CH2:25][C:14]([C:13]([O:18][CH3:19])=[O:17])([CH3:16])[CH3:15])=[CH:23][CH:22]=1

Participants

8

Reactant 5

HCID 311Citric AcidHCID 7912DiisopropylamineHCID 11039Methyl isobutyrateHCID 685274-Bromobenzyl bromideHCID 178418339Butyllithium

Product 1

HCID 22503289Methyl 4-bromo-α,α-dimethylbenzenepropanoateYield 71.9%

Reagents, catalysts & solvents 2

HCID 8028TetrahydrofuranSolventHCID 8058HexaneSolvent

Conditions

Temperature
-70 °C

Procedure

A 1.25M solution of n-butyl lithium in hexane (32 ml) was cooled to 0° C. under an argon atmosphere and diisopropylamine (4.05 g; 5.24 ml) was added slowly. The resulting mixture was cooled to −70° C. and stirred while methyl isobutyrate (4.08 g; 4.58 ml) was added dropwise while maintaining the temperature at <−60° C. After a further 30 minutes at −70° C., a solution of 4-bromobenzyl bromide (10.0 g) in anhydrous tetrahydrofuran (20 ml) was added and the temperature was maintained at −70° C. for a further 1.5 hours. The reaction mixture was allowed to attain ambient temperature then heated to reflux for 18 hours. On cooling, the mixture was acidified with 8% aqueous citric acid and extracted with ethyl acetate (3×75 ml). Insoluble material at the interface was removed by filtration and the combined organic phase was washed with brine (20 ml), dried (MgSO4) and evaporated. The residue was purified by vacuum flash chromatography on silica eluting with a gradient of 0-10% ethyl acetate in hexane to give 1-bromo-4-(2-methoxycarbonyl-2-methylpropyl)benzene (7.79 g); 1H NMR (d6-DMSO): 1.13 (s, 6H); 2.79 (s, 2H), 3.60 (s, 3H), 7.04 (m, 2H), 7.46 (d of t, 2H); mass spectrum (CI+): 272 (M+H)+.

Workup

  1. additionwas added dropwise
  2. temperaturewhile maintaining the temperature at <−60° C
  3. temperaturethe temperature was maintained at −70° C. for a further 1.5 hours
  4. customto attain ambient temperature
  5. temperaturethen heated
  6. temperatureto reflux for 18 hours
  7. temperatureOn cooling
  8. extractionextracted with ethyl acetate (3×75 ml)
  9. customInsoluble material at the interface was removed by filtration
  10. washthe combined organic phase was washed with brine (20 ml)
  11. dry with materialdried (MgSO4)
  12. customevaporated
  13. customThe residue was purified by vacuum flash chromatography on silica eluting with a gradient of 0-10% ethyl acetate in hexane

Sources & evidence

ORD record
ord-d6045b15d933436eaab03595e82e2c57
Source dataset
uspto-grants-2001_07
Patent number
US06258817B1

Reaction notes

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