Trifluoroacetic acid → L-alanine, 2-(benzyloxycarbonylamino)ethyl amide

HRID 234089Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 234089
[CH2:1]([O:8][C:9]([NH:11][CH2:12][CH2:13][NH:14][C:15](=[O:26])[C@H:16]([CH3:25])[NH:17]C(OC(C)(C)C)=O)=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.FC(F)(F)C(O)=O>ClCCl>[CH2:1]([O:8][C:9]([NH:11][CH2:12][CH2:13][NH:14][C:15](=[O:26])[C@H:16]([CH3:25])[NH2:17])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Komponenten

4

Edukt 2

HCID 6422Trifluoroacetic acidHCID 54526617HCID 54526617, Verbindung

Produkt 1

HCID 57139072L-alanine, 2-(benzyloxycarbonylamino)ethyl amideAusbeute 90 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

A solution of 12.0 g (0.033 mol) of (1g) in 25 ml of dichloromethane was cooled with an ice bath and 25 ml of trifluoroacetic acid was added. The solution was stirred at ca 5° C. for 20 minutes, then allowed to stir to room temperature. After 90 minutes, the dichloromethane and trifluoroacetic acid were removed in vacuo. The resulting residue was dissolved in 200 ml of ethyl acetate and washed with 2M sodium hydroxide (200 ml) and brine (100 ml). After drying over anhydrous magnesium sulfate, the solution was filtered and concentrated in vacuo to produce 7.86 g (90% yield) of L-alanine, 2-(benzyloxycarbonylamino)ethyl amide (1h) as a white solid. 1H NMR (CDCl3) δ 1.28(d, 3H), 2.09(m, 2H), 3.33(m, 4H), 3.47(q, 1H), 5.07(s, 2H), 5.59(bt, 1H), 7.33(bs, 5H), 7.69(bt, 1H); 13C NMR (CDCl3) δ 21.3, 39.5, 40.9, 50.4, 66.6, 128.0, 128.1, 128.4, 136.4, 156.9, 176.7.

Aufarbeitung

  1. stirringto stir to room temperature
  2. waitAfter 90 minutes
  3. customthe dichloromethane and trifluoroacetic acid were removed in vacuo
  4. dissolutionThe resulting residue was dissolved in 200 ml of ethyl acetate
  5. washwashed with 2M sodium hydroxide (200 ml) and brine (100 ml)
  6. dry with materialAfter drying over anhydrous magnesium sulfate
  7. filtrationthe solution was filtered
  8. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-ab7b031a9d16475b99e275fd38030da7
Quelldatensatz
uspto-grants-1997_01
Patentnummer
US05594106

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