Trifluoroacetic acid → Trifluoroacetate

HRID 1642058Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1642058
[CH2:1]([O:3][C:4](=[O:24])[CH2:5][N:6]([C:15]1[CH:20]=[CH:19][CH:18]=[C:17]([N+:21]([O-:23])=[O:22])[CH:16]=1)[S:7]([NH:10]C(C)(C)C)(=[O:9])=[O:8])[CH3:2].[C:25]([OH:31])([C:27]([F:30])([F:29])[F:28])=[O:26]>O1CCOCC1>[CH2:1]([O:3][C:4](=[O:24])[CH2:5][N:6]([C:15]1[CH:20]=[CH:19][CH:18]=[C:17]([N+:21]([O-:23])=[O:22])[CH:16]=1)[S:7]([NH2:10])(=[O:9])=[O:8])[CH3:2].[F:28][C:27]([F:30])([F:29])[C:25]([O-:31])=[O:26]

Komponenten

5

Versuchsvorschrift

5 mmol of (3-nitro-phenyl-N-(t-butylaminosulfonyl)amino)-acetic acid ethyl ester is dissolved in 20 ml of 90% aqueous TFA and the mixture obtained is stirred for 1 hour at rt. The mixture obtained is diluted with dioxane and solvent is evaporated. (3-Nitro-phenyl-N-(aminosulfonyl)amino)-acetic acid ethyl ester in the form of a trifluoroacetate is obtained.

Aufarbeitung

  1. customthe mixture obtained
  2. customThe mixture obtained
  3. customis evaporated

Quellen und Nachweise

ORD-Eintrag
ord-33cc340f28a9432b8d1dfeb5c7afd54e
Quelldatensatz
uspto-grants-2012_02
Patentnummer
US08119617B2

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