Reaktion #66272

ord-3cf4e12ef20e427cba563ac0e925fe95

Reaktionsgleichung

CCCN
propylamine
CC1(C)OCC(C=O)O1
2,2-dimethyl-1,3-dioxolane-4-carbaldehyde
CC(=O)O[BH-](OC(C)=O)OC(C)=O.[Na+]
sodium triacetoxyborohydride
CCCNCC1COC(C)(C)O1
N-((2,2-dimethyl-1,3-dioxolan-4-yl)methyl)propan-1-amine
Ausbeute 94.4%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe reaction mixture was then quenched with sat'd aq NaHCO3
  2. 2
    Extraktionextracted with EtOAc
  3. 3
    TrocknenThe organic layer was dried with MgSO4
  4. 4
    Filtrationfiltered
  5. 5
    Einengenconcentrated under reduced pressure
  6. 6
    Sonstigeto give the crude material that
  7. 7
    Sonstigewas purified by silica gel flash column chromatography (CH2Cl2 to 10% MeOH in CH2Cl2, gradient)

Vorschrift

To a solution of propylamine (0.72 mL, 7.7 mmol) and 2,2-dimethyl-1,3-dioxolane-4-carbaldehyde (1.0 g, 7.7 mmol) in 1,2-dichloroethane (25 mL) was added sodium triacetoxyborohydride (2.28 g, 10.8 mmol). The mixture was stirred for 1.5 h at room temperature. The reaction mixture was then quenched with sat'd aq NaHCO3 and extracted with EtOAc. The organic layer was dried with MgSO4, filtered, and concentrated under reduced pressure to give the crude material that was purified by silica gel flash column chromatography (CH2Cl2 to 10% MeOH in CH2Cl2, gradient) to afford 1.26 g (73%) of N-((2,2-dimethyl-1,3-dioxolan-4-yl)methyl)propan-1-amine.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08524702B2uspto-grants-2013_09