Réaction #155435

Équation de réaction

2-oxazolidinone

triphosgene

2-fluoro-4-hydroxybenzaldehyde

triethylamine

triethylamine

→

3-fluoro-4-formylphenyl 2-oxooxazolidine-3-carboxylate

Rendement 126.0%

Solvants

THF

CH2Cl2

MTBE

water

Conditions de réaction

Traitement

1. 1
   AutreTo a 250 mL dry round bottom flask
2. 2
   workup.STIRRINGAfter stirring at 0° C. for 1 hour
3. 3
   workup.STIRRINGthe mixture was stirred continually at room temperature overnight
4. 4
   FiltrationThe reaction mixture was filtered
5. 5
   Concentrationthe filtrate was concentrated
6. 6
   workup.DISSOLUTIONThe residue was dissolved in 10 mL of CH2Cl2
7. 7
   workup.STIRRINGAfter stirring at room temperature for 2 days
8. 8
   FiltrationThe mixture was filtered
9. 9
   Lavagethe solid was washed with cold water (50 mL×2)
10. 10
    Extractionfollowed by extraction
11. 11
    AutreAfter drying

Mode opératoire

To a 250 mL dry round bottom flask were added 2-oxazolidinone (4.35 g, 50.0 mmol), triphosgene (5.49 g, 18.5 mmol) and anhydrous THF (100 mL). The mixture was stirred in an ice-water bath, then triethylamine (9.8 mL, 70.0 mmol) was added slowly. After stirring at 0° C. for 1 hour, the mixture was stirred continually at room temperature overnight. The reaction mixture was filtered and the filtrate was concentrated. The residue was dissolved in 10 mL of CH2Cl2, and this solution was added slowly to a stirring mixture of 2-fluoro-4-hydroxybenzaldehyde (3.78 g, 27.0 mmol) and triethylamine (5.63 mL, 40.4 mmol) in 20 mL of anhydrous CH2Cl2 at 0° C. After stirring at room temperature for 2 days, water (80 mL) and MTBE (100 mL) were added to the reaction mixture. The mixture was filtered and the solid was washed with cold water (50 mL×2), followed by extraction using MTBE (50 mL×4). After drying, 3-fluoro-4-formylphenyl 2-oxooxazolidine-3-carboxylate (5.90 g) was obtained as a white solid. Yield: 86%. 1H NMR (CDCl3, 300 MHz): δ=10.42 (s, 1H), 8.03 (t, J=8.1 Hz, 1H), 7.27-7.23 (m, 2H), 4.61 (t, J=7.8 Hz, 2H), 4.29 (t, J=7.5 Hz, 2H). 13C NMR (CDCl3, 75.5 MHz): δ=186.3 (d, J=6.0 Hz), 166.9, 155.0 (d, J=260 Hz), 130.2, 122.6, 118.3, 110.7 (d, J=24.4 Hz), 62.2, 43.9. 19F NMR (CDCl3, 282.3 MHz): δ=−118.6.

Source