4-Methoxybenzenesulfonyl chloride → N-[4-methoxybenzenesulfonyl]-(D)-valine

HRID 264328

Reaktionsgleichung

Reaktionsgleichung von HRID 264328
[NH2:1][C@@H:2]([C:6]([OH:8])=[O:7])[CH:3]([CH3:5])[CH3:4].C(N(CC)CC)C.[CH3:16][O:17][C:18]1[CH:23]=[CH:22][C:21]([S:24](Cl)(=[O:26])=[O:25])=[CH:20][CH:19]=1>O.CC(C)=O>[CH3:16][O:17][C:18]1[CH:19]=[CH:20][C:21]([S:24]([NH:1][C@@H:2]([C:6]([OH:8])=[O:7])[CH:3]([CH3:5])[CH3:4])(=[O:26])=[O:25])=[CH:22][CH:23]=1

Komponenten

6

Versuchsvorschrift

To a solution of D-valine (2000 g, 17.09 mol) in water (16.9 L) and acetone (9.5 L), cooled to 5° C., is added triethylamine (4769 mL, 34.22 mol), and the reaction is stirred for 30 minutes. Then a solution of 4-methoxybenzenesulfonyl chloride (3524 g, 18.48 mol) in acetone (7.4 L) is added over 30 minutes, and the reaction is stirred at room temperature overnight. Most of the acetone is evaporated off, and the pH is adjusted to pH=8.25 with 6N sodium hydroxide. The crude product is washed with toluene (2×10 L), and then the pH is re-adjusted to pH=2.2 with 6N hydrochloric acid. The mixture is then extracted with methylene chloride (3×12 L), the combined organic layers are washed with 2N hydrochloric acid, water, dried (Na2SO4), and the solvent is evaporated to provide N-[4-methoxybenzenesulfonyl]-(D)-valine.

Aufarbeitung

  1. stirringthe reaction is stirred at room temperature overnight
  2. customMost of the acetone is evaporated off
  3. washThe crude product is washed with toluene (2×10 L)
  4. extractionThe mixture is then extracted with methylene chloride (3×12 L)
  5. washthe combined organic layers are washed with 2N hydrochloric acid, water
  6. dry with materialdried (Na2SO4)
  7. customthe solvent is evaporated

Quellen und Nachweise

ORD-Eintrag
ord-fe170c181c9740b480664bb7da84a39b
Quelldatensatz
uspto-grants-1997_07
Patentnummer
US05646167

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