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Trifluoroacetic acid → (S)-methyl 2-(ethylamino)propanoate

HRID 2077854
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2077854
C(OC([N:8]([CH2:15][CH3:16])[C@@H:9]([CH3:14])[C:10]([O:12][CH3:13])=[O:11])=O)(C)(C)C.C(O)(C(F)(F)F)=O>ClCCl>[CH2:15]([NH:8][C@@H:9]([CH3:14])[C:10]([O:12][CH3:13])=[O:11])[CH3:16]
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Komponenten

4

Edukt 2

HCID 6422Trifluoroacetic acidHCID 58324365(S)-methyl 2-(tert-butoxycarbonyl(ethyl)amino)propanoate

Produkt 1

HCID 43230256(S)-methyl 2-(ethylamino)propanoate

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

(S)-methyl 2-(tert-butoxycarbonyl(ethyl)amino)propanoate (4.40 g, 19.0 mmol) was dissolved in dichloromethane and treated with TFA (10 mL). The reaction mixture was stirred for 2 h at room temperature and concentrated in vacuo. The residue was diluted with brine and NaOH (aq. 50%) was added dropwise until pH=12.5. This was extracted with EtOAc (3×30 mL). The combined organic extracts were dried (MgSO4), filtered and concentrated in vacuo to afford the title compound as an opaque liquid (1.85 g, 74%). [M+H] calc'd for C6H13NO2, 132; found, 132.

Aufarbeitung

  1. concentrationconcentrated in vacuo
  2. additionThe residue was diluted with brine and NaOH (aq. 50%)
  3. additionwas added dropwise until pH=12.5
  4. extractionThis was extracted with EtOAc (3×30 mL)
  5. dry with materialThe combined organic extracts were dried (MgSO4)
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-9fc6765b61b2444184da08179b7e4cb0
Quelldatensatz
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07928105B2

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