1,8-Diazabicyclo(5.4.0)undec-7-ene → 3-(Azidomethyl)-5-chloro-2-methylpyridine
Reaktionsgleichung
[Cl:1][C:2]1[CH:3]=[C:4]([CH2:9]O)[C:5]([CH3:8])=[N:6][CH:7]=1.C1(P([N:25]=[N+:26]=[N-:27])(C2C=CC=CC=2)=O)C=CC=CC=1.N12CCCN=C1CCCCC2>C1(C)C=CC=CC=1>[N:25]([CH2:9][C:4]1[C:5]([CH3:8])=[N:6][CH:7]=[C:2]([Cl:1])[CH:3]=1)=[N+:26]=[N-:27]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 0 °C
Versuchsvorschrift
To a stirring solution of 399 mg (2.55 mmol) of (5-chloro-2-methylpyridin-3-yl)methanol in 10 mL of toluene at r.t. was added 660 μL (3.06 mmol) of DPPA (diphenylphosphoryl azide). The solution was cooled to 0° C. and 450 μL of DBU (1,8-diazabicyclo[5.4.0]undec-7-ene) was added. The ice bath was removed and stirring was continued with warming to r.t. After 16 h, 1 N HCl was added to a pH=8. Water was added and the aqueous layer was extracted with EtOAc. The organic layer was washed with brine, dried over Na2SO4, filtered, and concentrated. Purification by flash silica gel chromatography (45% EtOAc/hexanes) provided 3-(azidomethyl)-5-chloro-2-methylpyridine as a yellow oil in quantitative yield.
Aufarbeitung
- customThe ice bath was removed
- temperaturewith warming to r.t
- addition1 N HCl was added to a pH=8
- additionWater was added
- extractionthe aqueous layer was extracted with EtOAc
- washThe organic layer was washed with brine
- dry with materialdried over Na2SO4
- filtrationfiltered
- concentrationconcentrated
- customPurification by flash silica gel chromatography (45% EtOAc/hexanes)
Quellen und Nachweise
- ORD-Eintrag
- ord-d42a839719bc4f12ab3b671dc2b2b436
- Quelldatensatz
- uspto-grants-2012_10
- Patentnummer
- US08299267B2
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