반응 #220919

반응 방정식

4-acetamidophenol

sodium hydride

(2R)-3-bromo-2-hydroxy-2-methyl-N-(3-methyl-4-nitrophenyl)propionamide

→

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

용매

THF

THF

THF

반응 조건

후처리

1. 1
   workup.ADDITIONthe temperature was kept below 5° C. during the addition
2. 2
   workup.STIRRINGThe mixture was stirred at room temperature for 30 min
3. 3
   workup.WAITat 60° C. for 5 h
4. 4
   기타The solvent was evaporated
5. 5
   workup.DISSOLUTIONthe residue was dissolved to the mixture of water (80 ml) and ethyl acetate (80 ml)
6. 6
   기타the phases were separated
7. 7
   세척The organic phase was washed with 1 M Na2CO3 (6×30 ml)
8. 8
   건조dried over Na2SO4
9. 9
   기타evaporated
10. 10
    기타The oily residue was crystallised from ethyl acetate

실험 절차

A solution of 4-acetamidophenol 0.62 g, 4.1 mmol) in THF (7 ml) was added dropwise to a stirred suspension of sodium hydride (0.27 g, 6.8 mmol, 60% dispersion in mineral oil) in THF (6 ml) and the temperature was kept below 5° C. during the addition. The mixture was stirred for 10 min and a solution of (2R)-3-bromo-2-hydroxy-2-methyl-N-(3-methyl-4-nitrophenyl)propionamide (0.86 g, 2.7 mmol) in THF (7 ml) was added. The mixture was stirred at room temperature for 30 min and then at 60° C. for 5 h, and allowed to cool to the room temperature. The solvent was evaporated and the residue was dissolved to the mixture of water (80 ml) and ethyl acetate (80 ml). The pH was adjusted to 2-3 with 2 M HCl and the phases were separated. The organic phase was washed with 1 M Na2CO3 (6×30 ml), dried over Na2SO4 and evaporated. The oily residue was crystallised from ethyl acetate. The yield was 0.27 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).

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