Реакция #1854075

Уравнение реакции

4-methoxybenzyl chloride

sodium 4-hydroxybutyrate

N,N-dimethylformamide

allyl 4-chloro-4-oxobutyrate

triethylamine

→

title compound

Выход 70.0%

Allyl 4-[(4-methoxybenzyl)oxy]-4-oxobutyl succinate

Выход 70.0%

Растворители

ethyl acetate

ethyl acetate

hexane

Условия реакции

Обработка

1. 1
   ТемператураThe reaction mixture was cooled
2. 2
   Другоеat 0° C
3. 3
   Промывкаthe resulting solution was washed successively with water
4. 4
   СушкаThe solution was dried over anhydrous magnesium sulfate
5. 5
   workup.DISTILLATIONthe solvent was distilled off under reduced pressure
6. 6
   Другоеto give an oily residue

Методика

To a suspension of commercially available sodium 4-hydroxybutyrate (756 mg, 6.00 mmol) in N,N-dimethylformamide (10 ml) was added 4-methoxybenzyl chloride (987 mg, 6.30 mmol), and the mixture was heated at 100° C. for 3 hours. The reaction mixture was cooled, and allyl 4-chloro-4-oxobutyrate (1.06 g, 6.02 mmol) obtained from Example 14-(1), triethylamine (920 μl, 6.60 mmol), and 4-(N,N-dimethylamino)pyridine (10 mg) were added thereto at 0° C. The mixture was stirred at room temperature for 18 hours, and the obtained mixture was diluted with ethyl acetate, then the resulting solution was washed successively with water, a saturated aqueous solution of sodium hydrogen carbonate, a saturated aqueous solution of ammonium chloride, and an aqueous solution of sodium chloride. The solution was dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure to give an oily residue. The residue was subjected to chromatography on a silica gel (50 g) column (eluent; hexane:ethyl acetate=3:1˜2:1) to afford the title compound (1.52 g, 70% yield) as a colorless oil.

Источник