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Sodium Azide → (+/-)-1-Methoxy-2-butyl Azide

HRID 1279270
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1279270
CS(O[CH:6]([CH2:10][CH3:11])[CH2:7][O:8][CH3:9])(=O)=O.[N-:12]=[N+:13]=[N-:14].[Na+]>CN(C=O)C>[CH3:9][O:8][CH2:7][CH:6]([N:12]=[N+:13]=[N-:14])[CH2:10][CH3:11]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 33557Sodium AzideHCID 22273165(+/-)-1-Methoxy-2-butanol Methanesulfonate

Produkt 1

HCID 18689797(+/-)-1-Methoxy-2-butyl Azide

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Reaktionsbedingungen

Temperatur
57.5 °C

Versuchsvorschrift

A solution of crude mesylate 1 (90.0 g, 0.495 mol) in DMF (500 mL) was treated with NaN3 (48.22g, 0.74 mol, 1.5 equiv) at 25° C. under N2. The resulting reaction mixture was warmed to 55-60° C. for 6-8 h with stirring before being quenched with H2O (500 mL). The pale-yellow solution was then extracted with EtOAc or Et2O (4×200 mL). The combined EtOAc (or Et2O) extracts were washed with H2O (3×500 mL), dried (MgSO4), and concentrated in vacuo. The residual solution was found to contain desired azide 2 (60.3 g, 64.5 g theoretical, 94%), which was found to be pure enough and directly used in the following reaction without further purification.

Aufarbeitung

  1. customThe resulting reaction mixture
  2. custombefore being quenched with H2O (500 mL)
  3. extractionThe pale-yellow solution was then extracted with EtOAc or Et2O (4×200 mL)
  4. washThe combined EtOAc (or Et2O) extracts were washed with H2O (3×500 mL)
  5. dry with materialdried (MgSO4)
  6. concentrationconcentrated in vacuo
  7. customdirectly used in the following reaction without further purification

Quellen und Nachweise

ORD-Eintrag
ord-f134f37cef8549998671f490a3d8fda0
Quelldatensatz
uspto-grants-2002_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06448261B1

Notizen zur Reaktion

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