Dimethyl Sulfoxide → 4-Nitropicolinaldehyde

HRID 600264Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 600264
C(Cl)(=O)C(Cl)=O.CS(C)=O.[N+:11]([C:14]1[CH:19]=[CH:18][N:17]=[C:16]([CH2:20][OH:21])[CH:15]=1)([O-:13])=[O:12].C(N(CC)CC)C>C(Cl)Cl.[Cl-].[Na+].O>[N+:11]([C:14]1[CH:19]=[CH:18][N:17]=[C:16]([CH:20]=[O:21])[CH:15]=1)([O-:13])=[O:12]

Komponenten

7

Reaktionsbedingungen

Temperatur
-78 °C

Versuchsvorschrift

To cooled solution of oxalyl chloride (0.533 g, 4.18 mmol) in DCM (2 mL) at −78° C. under nitrogen was added dimethyl sulfoxide (0.593 mL, 8.37 mmol) dropwise. After 30 minutes (4-nitro-pyridin-2-yl)-methanol (17)(0.129, 0.837 mmol) in DCM (2 mL) was added dropwise maintaining temperature at −78° C. After 2 hours the mixture was warmed to −55° C. Triethylamine (1.74 mL, 12.55 mmol) was then added and the mixture allowed to warm to room temperature over 2 hours. Brine (10 mL) was then added and the mixture extracted with DCM (4×10 mL). The combined organics were then dried over MgSO4 and concentrated in vacuo to an oil. The material was used directly without need for purification assuming quantitative conversion.

Aufarbeitung

  1. temperatureAfter 2 hours the mixture was warmed to −55° C
  2. temperatureto warm to room temperature over 2 hours
  3. extractionthe mixture extracted with DCM (4×10 mL)
  4. dry with materialThe combined organics were then dried over MgSO4
  5. concentrationconcentrated in vacuo to an oil
  6. customThe material was used directly without need for purification

Quellen und Nachweise

ORD-Eintrag
ord-1e9d636496704bfaac3c279886c4075c
Quelldatensatz
uspto-grants-2011_03
Patentnummer
US07902193B2

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