Citric Acid → Methyl 3-(4-bromophenyl)-2,2-dimethylpropanoate

HRID 1378357Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1378357
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>[CH3:19][O:18][C:13]([C:14]([CH3:16])([CH3:15])[CH2:25][C:24]1[CH:27]=[CH:28][C:21]([Br:20])=[CH:22][CH:23]=1)=[O:17]

Komponenten

8

Edukt 5

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

Produkt 1

HCID 22503289Methyl 3-(4-bromophenyl)-2,2-dimethylpropanoateAusbeute 71,9 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 8028TetrahydrofuranLösungsmittelHCID 8058HexaneLösungsmittel

Reaktionsbedingungen

Temperatur
-70 °C

Versuchsvorschrift

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 (Mg SO4) and evaporated. The residue was subjected to vacuum flash chromatography on silica eluting with a gradient of 0-10% ethyl acetate in hexane to give 4-(2-methoxycarbonyl-2-methylpropyl)bromobenzene (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)+.

Aufarbeitung

  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 (Mg SO4)
  12. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-4d213ac59691448bb932eceaa676d540
Quelldatensatz
uspto-grants-1997_09
Patentnummer
US05668137

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