Réaction #155432

Équation de réaction

2,6-difluoro-4-hydroxybenzaldehyde

5,5-dimethyl-oxazolidin-2-one

triphosgene

triethylamine

triethylamine

→

3,5-difluoro-4-formylphenyl 5,5-dimethyl-2-oxooxazolidine-3-carboxylate

Rendement 130.3%

Solvants

water

CH2Cl2

THF

Conditions de réaction

Traitement

1. 1
   AutreTo a 250 mL dry round bottom flask
2. 2
   workup.STIRRINGThe resulting mixture was stirred at room temperature overnight
3. 3
   FiltrationThe reaction mixture was filtered
4. 4
   Concentrationthe filtrate was concentrated
5. 5
   TempératureThe resulting solution was cooled in an ice-water bath
6. 6
   workup.STIRRINGAfter stirring at room temperature for 7 hours
7. 7
   AutreThe CH2Cl2 layer was separated
8. 8
   Extractionthe aqueous layer was extracted continually with CH2Cl2 (50 mL×3)
9. 9
   SéchageThe combined CH2Cl2 solution was dried over Na2SO4
10. 10
    AutreAfter removal of the solvent
11. 11
    Autrethe residue was purified with a silica gel chromatography (heptane/ethyl acetate, gradient eluting)

Mode opératoire

To a 250 mL dry round bottom flask were added 5,5-dimethyl-oxazolidin-2-one (5.10 g, 44.3 mmol), triphosgene (5.26 g, 17.7 mmol) and anhydrous THF (80 mL). The mixture was stirred in an ice-water bath, then triethylamine (8.6 mL, 62.0 mmol) was added slowly. The resulting mixture was stirred at room temperature overnight. The reaction mixture was filtered and the filtrate was concentrated. To the residue was added 2,6-difluoro-4-hydroxybenzaldehyde (5.03 g, 31.9 mmol) and 80 mL of CH2Cl2. The resulting solution was cooled in an ice-water bath, then triethylamine (6.0 mL, 42.5 mmol) was added. After stirring at room temperature for 7 hours, water (100 mL) was added to the reaction mixture. The CH2Cl2 layer was separated, and the aqueous layer was extracted continually with CH2Cl2 (50 mL×3). The combined CH2Cl2 solution was dried over Na2SO4. After removal of the solvent, the residue was purified with a silica gel chromatography (heptane/ethyl acetate, gradient eluting) to give 3,5-difluoro-4-formylphenyl 5,5-dimethyl-2-oxooxazolidine-3-carboxylate (6.9 g) as a pale yellow crystal. Yield: 52%. 1H NMR (CDCl3, 300 MHz): δ=10.39 (s, 1H), 7.09 (d, J=9.0 Hz, 2H), 3.97 (s, 2H), 1.67 (s, 6H).

Source