تفاعل #155419

معادلة التفاعل

2,6-difluoro-4-hydroxybenzaldehyde

pyridine

2-oxazolidinone

triphosgene

triethylamine

→

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

المردود 98.1%

المذيبات

CH2Cl2

water

THF

ظروف التفاعل

المعالجة

1. 1
   أخرىTo 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
   ترشيحThe reaction mixture was filtered
5. 5
   تركيزthe filtrate was concentrated
6. 6
   workup.DISSOLUTIONThe residue was dissolved in 20 mL of CH2Cl2
7. 7
   workup.STIRRINGAfter stirring at room temperature for 10 hours
8. 8
   أخرىThe CH2Cl2 layer was separated
9. 9
   استخلاصthe aqueous layer was extracted continually with CH2Cl2 (50 mL×4)
10. 10
    تجفيفThe combined CH2Cl2 solution was dried over Na2SO4
11. 11
    أخرىAfter removal of the solvent
12. 12
    أخرىthe residue was purified with a silica gel chromatography (heptane/ethyl acetate, gradient eluting)

الإجراء التجريبي

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 (80 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 20 mL of CH2Cl2, and this solution was added slowly to a stirring mixture of 2,6-difluoro-4-hydroxybenzaldehyde (5.93 g, 27.5 mmol) and pyridine (4.44 mL, 55.0 mmol) in 30 mL of anhydrous CH2Cl2 at 0° C. After stirring at room temperature for 10 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×4). 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 2-oxooxazolidine-3-carboxylate (4.92 g) as a white solid. Yield: 33%. 1H NMR (CDCl3, 300 MHz): δ=10.29 (s, 1H), 6.98 (dd, J=10.8, 2.1 Hz, 2H), 4.51 (t, J=7.8 Hz, 2H), 4.18 (t, J=7.6 Hz, 2H). 13C NMR (CDCl3, 75.5 MHz): δ=183.5, 163.7 (dd, J=263.6, 8.00 Hz), 151.2, 148.0, 112.6, 106.8 (dd, J=25.7, 3.70 Hz), 62.1, 43.7.

المصدر