Tetrabutylammonium Fluoride → [2-(2-Hydroxyethoxy)ethoxy]methylcarbamic acid tert-butyl ester

HRID 2093242

Reaktionsgleichung

Reaktionsgleichung von HRID 2093242
CCCC[N+](CCCC)(CCCC)CCCC.[F-].C([Si](C1C=CC=CC=1)(C1C=CC=CC=1)[O:24][CH2:25][CH2:26][O:27][CH2:28][CH2:29][O:30][N:31]([CH3:39])[C:32]([O:34][C:35]([CH3:38])([CH3:37])[CH3:36])=[O:33])(C)(C)C>C1COCC1>[CH3:39][N:31]([C:32]([O:34][C:35]([CH3:38])([CH3:37])[CH3:36])=[O:33])[O:30][CH2:29][CH2:28][O:27][CH2:26][CH2:25][OH:24]

Komponenten

4

Edukt 2

HCID 2724141Tetrabutylammonium FluorideHCID 86643773O-{2-[2-(tert-Butyl-diphenyl-silanyloxy)-ethoxy]-ethyl}-N-methyl-N-BOC-hydroxylamine

Produkt 1

HCID 86643775[2-(2-Hydroxyethoxy)ethoxy]methylcarbamic acid tert-butyl ester

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

TBAF (6.78 mL, 6.78 mmol) was added to O-{2-[2-(tert-Butyl-diphenyl-silanyloxy)-ethoxy]-ethyl}-N-methyl-N-BOC-hydroxylamine (d) (3 g, 6.33 mmol) dissolved in dry THF (15 mL). The reaction was stirred over night. The THF was evaporated off and the residue was dissolved in DCM and washed with NH4Cl (saturated) (40 mL), water and brine. The organic phase was dried (MgSO4) and evaporated off. The residue was purified using flash chromatography on a Companion Combiflash 40 g column (Gradient MeOH 0-5% over 20 minutes in DCM. Structure confirmed by NMR.

Aufarbeitung

  1. customThe THF was evaporated off
  2. dissolutionthe residue was dissolved in DCM
  3. washwashed with NH4Cl (saturated) (40 mL), water and brine
  4. dry with materialThe organic phase was dried (MgSO4)
  5. customevaporated off
  6. customThe residue was purified
  7. customover 20 minutes

Quellen und Nachweise

ORD-Eintrag
ord-65ceeeb5788c4d60a7f0d86a84da181c
Quelldatensatz
uspto-grants-2013_05
Patentnummer
US08444955B2

Verknüpfte Notizen

Wird geladen…