Réaction #155427

Équation de réaction

4-morpholinecarbonyl chloride

3-fluoro-2-hydroxybenzaldehyde

CH2Cl2

pyridine

→

2-fluoro-6-formylphenyl morpholine-4-carboxylate

Rendement 94.1%

Solvants

Water

Conditions de réaction

Traitement

1. 1
   AutreTo a 250 mL dry round bottom flask
2. 2
   workup.STIRRINGThe mixture was stirred at room temperature for 24 hours
3. 3
   AutreThe CH2Cl2 layer was separated
4. 4
   Extractionthe aqueous layer was extracted continually with CH2Cl2 (100 mL×2)
5. 5
   SéchageThe combined CH2Cl2 solution was dried over Na2SO4
6. 6
   AutreAfter removal of the solvent
7. 7
   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 3-fluoro-2-hydroxybenzaldehyde (4.90 g, 35.0 mmol), anhydrous CH2Cl2 (50 mL) and pyridine (3.40 mL, 42.0 mmol). The mixture was stirred in an ice-water bath, then 4-morpholinecarbonyl chloride (4.50 mL, 38.5 mmol) was added. The mixture was stirred at room temperature for 24 hours. Water (80 mL) was added to the reaction mixture. The CH2Cl2 layer was separated, and the aqueous layer was extracted continually with CH2Cl2 (100 mL×2). 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 2-fluoro-6-formylphenyl morpholine-4-carboxylate (8.34 g) as white solid. Yield: 94%. 1H NMR (CDCl3, 300 MHz): δ=10.06 (s, 1H), 7.58 (dt, J=7.8, 1.5 Hz, 1H), 7.39-7.22 (m, 2H), 3.69 (br, 6H), 3.50 (br, 2H). 13C NMR (CDCl3, 75.5 MHz, mixture of two isomers): δ=187.6, 187.5, 170.5, 156.4, 152.4 (d, J=100.7 Hz), 139.9 (d, J=12.8 Hz), 130.5, 126.5 (d, J=7.3 Hz), 125.2 (d, J=3.1 Hz), 121.7 (d, J=17.4 Hz), 66.1, 45.0, 44.3.

Source