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Dichloromethane → (S)-2-((tert-butoxycarbonyl)amino)-3-(2-nitrophenoxy)propanoic acid

HRID 1187
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1187
[CH3:1][C:2]([CH3:14])([O:4][C:5]([NH:7][C@H:8]([C:11]([OH:13])=[O:12])[CH2:9][OH:10])=[O:6])[CH3:3].[H-].[Na+].F[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=1[N+:24]([O-:26])=[O:25].C(Cl)Cl>CN(C)C=O.C(O)(=O)C.CO>[CH3:3][C:2]([CH3:14])([O:4][C:5]([NH:7][C@H:8]([C:11]([OH:13])=[O:12])[CH2:9][O:10][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=1[N+:24]([O-:26])=[O:25])=[O:6])[CH3:1]
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Komponenten

8

Edukt 4

HCID 6344DichloromethaneHCID 24758Sodium hydrideHCID 738951-Fluoro-2-nitrobenzeneHCID 98766N-[tert-butoxycarbonyl]-L-serine

Produkt 1

HCID 18599736(S)-2-((tert-butoxycarbonyl)amino)-3-(2-nitrophenoxy)propanoic acid

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 176
Acetic Acid
Lösungsmittel
HCID 887MethanolLösungsmittel
HCID 6228DimethylformamideLösungsmittel2×

Versuchsvorschrift

A solution of N-[(1,1-dimethylethoxy)carbonyl]-L-serine (24.3 g., 0.118 mole) in dry dimethylformamide (25 ml.) was added dropwise over a period of 1.0 hour to a cooled (0°, ice-salt bath) suspension of 60% sodium hydride (10.1 g., 0.25 mole) in dry dimethylformamide (200 ml.) and stirring was continued at 0° until the frothing subsided (about 2.0 hours). The reaction mixture was treated dropwise with 1-fluoro-2-nitrobenzene (14.3 ml., 0.13 mole) over a period of 20 minutes, stirred at 0° under argon for 4.0 hours then poured into ice-water (750 ml.) and extracted with ethyl acetate (2×100 ml.). The aqueous phase was brought to pH 1.0 with 6N hydrochloric acid (70 ml.), extracted with ethyl acetate (3×500 ml.) and the combined organic extracts were washed with brine (100 ml.), dried (anhydrous sodium sulfate), filtered, evaporated to dryness and dried in vacuo. The crude product mixture was chromatographed on a silica gel column (Merck), eluting the column with methylene chloride:methanol:acetic acid (100:5:0.2) to give 27.22 g. of product as a thick yellow syrup; Rf =0.27 (methylene chloride:methanol:acetic acid, 100:5:0.5).

Aufarbeitung

  1. temperaturea cooled
  2. customwas continued at 0° until the frothing
  3. custom(about 2.0 hours)
  4. stirringstirred at 0° under argon for 4.0 hours
  5. extractionextracted with ethyl acetate (2×100 ml.)
  6. extractionextracted with ethyl acetate (3×500 ml.)
  7. washthe combined organic extracts were washed with brine (100 ml.)
  8. dry with materialdried (anhydrous sodium sulfate)
  9. filtrationfiltered
  10. customevaporated to dryness
  11. customdried in vacuo
  12. customThe crude product mixture was chromatographed on a silica gel column (Merck)
  13. washeluting the column with methylene chloride:methanol:acetic acid (100:5:0.2)
  14. customto give 27.22 g

Quellen und Nachweise

ORD-Eintrag
ord-c2956910e6964c68a222931d19fd2abc
Quelldatensatz
uspto-grants-1998_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05723457

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