Réaction #220913

Équation de réaction

4-acetamidophenol

sodium hydride

2-methyl-oxirane-2-carboxylic acid (3-methyl-4-nitrophenyl)amide

→

3-(4-Acetylaminophenoxy)-2-hydroxy-2-methyl-N-(3-methyl-4-nitrophenyl)propionamide

Solvants

THF

THF

THF

Conditions de réaction

Traitement

1. 1
   workup.ADDITIONthe temperature was kept below 5° C. during the addition
2. 2
   workup.STIRRINGstirred at this temperature for 7 h
3. 3
   Températureto cool to the room temperature
4. 4
   AutreThe solvent was evaporated
5. 5
   workup.DISSOLUTIONthe residue was dissolved to the mixture of water (150 ml) and ethyl acetate (150 ml)
6. 6
   Autrethe phases were separated
7. 7
   ExtractionThe aqueous phase was extracted with ethyl acetate (4×150 ml)
8. 8
   LavageThe combined organic phase was washed with 1 M Na2CO3 (5×100 ml)
9. 9
   Séchagedried over Na2SO4
10. 10
    Autreevaporated
11. 11
    AutreThe oily residue was crystallised from the mixture of ethyl acetate-diethyl ether (10:1)
12. 12
    AutreThe crude product was recrystallised from ethyl acetate

Mode opératoire

A solution of 4-acetamidophenol (2.9 g, 19 mmol) in THF (60 ml) was added dropwise to a stirred suspension of sodium hydride (0.46 g, 19 mmol, 60% dispersion in mineral oil) in THF (60 ml) and the temperature was kept below 5° C. during the addition. The mixture was stirred for 10 min and a solution of 2-methyl-oxirane-2-carboxylic acid (3-methyl-4-nitrophenyl)amide (3.05 g, 13 mmol) in THF (120 ml) was added. The mixture was heated to 60° C. and stirred at this temperature for 7 h, and allowed to cool to the room temperature. The solvent was evaporated and the residue was dissolved to the mixture of water (150 ml) and ethyl acetate (150 ml). The pH was adjusted to 2-3 with 2 M HCl and the phases were separated. The aqueous phase was extracted with ethyl acetate (4×150 ml). The combined organic phase was washed with 1 M Na2CO3 (5×100 ml), dried over Na2SO4 and evaporated. The oily residue was crystallised from the mixture of ethyl acetate-diethyl ether (10:1). The crude product was recrystallised from ethyl acetate. The yield was 2.5 g. 1H NMR (DMSO-d6): 1.42 (3H, s), 1.99 (3H, s), 2.53 (3H, s), 3.93 (1H, d, J=9.6 Hz), 4.16 (1H, d, J=9.6 Hz), 6.20 (1H, bs), 6.84 (2H, d, J=9.0 Hz), 7.44 (2H, d, J=9.0 Hz), 7.88 (1H, dd, J=9.0 Hz and 2.3 Hz), 7.93 (1H, d, J=2.3 Hz), 8.04 (1H, d, J=9.0 Hz), 9.76 (1H, s), 10.15 (1H, bs).

Source