Реакция #9615

Уравнение реакции

bromobenzene

3,3-dimethyldihydro-2,5-furandione

aluminum

→

4-(4-bromophenyl)-2,2-dimethyl-4-oxobutanoic acid

Выход 63.0%

Растворители

dichloroethane

Условия реакции

Обработка

1. 1
   ДругоеThe ice bath was removed
2. 2
   ТемператураThe mixture was again chilled in an ice/water bath
3. 3
   Другоеquenched with 1 M aqueous hydrochloric acid
4. 4
   workup.ADDITIONWater (70 mL) was added
5. 5
   Другоеthe layers were separated
6. 6
   ЭкстракцияThe aqueous layer was extracted with ethyl acetate (3×50 mL)
7. 7
   СушкаThe combined organic layers were dried over anhydrous magnesium sulfate
8. 8
   Концентрированиеconcentrated under reduced pressure
9. 9
   ДругоеThe residue was purified by flash chromatography (Biotage apparatus, 17:83 ethyl acetate/hexane)

Методика

To a chilled solution (ice/water bath) of bromobenzene (7.71 g, 49.1 mmol) and 3,3-dimethyldihydro-2,5-furandione (5.99 g, 46.7 mmol) in dichloroethane (150 mL) was added aluminum trichworide (13.28 g, 99.58 mmol). The ice bath was removed and the reaction mixture was stirred at rt overnight. The mixture was again chilled in an ice/water bath, and then quenched with 1 M aqueous hydrochloric acid. Water (70 mL) was added and the layers were separated. The aqueous layer was extracted with ethyl acetate (3×50 mL). The combined organic layers were dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by flash chromatography (Biotage apparatus, 17:83 ethyl acetate/hexane) to give 4-(4-bromophenyl)-2,2-dimethyl-4-oxobutanoic acid as a white solid (8.34 g, 63%). LC-MS: ret. time 2.79 min; m/z 284.8 (MH+); 1H NMR (300 MHz, CDCl3) δ 1.36 (s, 6H), 3.27 (s, 2H), 7.60 (d, 2H), 7.81 (d, 2H).

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