Trifluoroacetic acid → 1-(3-((Tert-butyldimethylsilyl)oxy)propyl)-1-methylhydrazine 2,2,2-trifluoroacetate

HRID 240726Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 240726
C(OC([NH:8][N:9]([CH2:11][CH2:12][CH2:13][O:14][Si:15]([C:18]([CH3:21])([CH3:20])[CH3:19])([CH3:17])[CH3:16])[CH3:10])=O)(C)(C)C.[F:22][C:23]([F:28])([F:27])[C:24]([OH:26])=[O:25]>ClCCl>[F:22][C:23]([F:28])([F:27])[C:24]([OH:26])=[O:25].[C:18]([Si:15]([CH3:16])([CH3:17])[O:14][CH2:13][CH2:12][CH2:11][N:9]([CH3:10])[NH2:8])([CH3:21])([CH3:20])[CH3:19]

Komponenten

4

Edukt 2

HCID 6422Trifluoroacetic acidHCID 86678100N'-[3-(t-Butyl-dimethyl-silanyloxy)-propyl]-N'-methyl-hydrazinecarboxylic acid t-butyl ester

Produkt 1

HCID 866781021-(3-((Tert-butyldimethylsilyl)oxy)propyl)-1-methylhydrazine 2,2,2-trifluoroacetate

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

N′-[3-(t-Butyl-dimethyl-silanyloxy)-propyl]-N′-methyl-hydrazinecarboxylic acid t-butyl ester (120 mg, 377 μmol) was at 0° C. combined with dichloromethane (2 mL) and trifluoroacetic acid (2 mL) to give a light yellow solution. The reaction mixture was stirred for 2 h at 0° C. and subsequently concentrated in vacuo to give the title compound as yellow oil, which was used without further purification in the next step.

Aufarbeitung

  1. customwas at 0° C.
  2. customto give a light yellow solution
  3. concentrationsubsequently concentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-ef25a6c26f5340ba87cf0ebfd96acc6d
Quelldatensatz
uspto-grants-2014_02
Patentnummer
US08648099B2

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