Formic Acid → 5-Bromo-2-formylaminomethylthiazole

HRID 230030

Reaktionsgleichung

Reaktionsgleichung von HRID 230030
Cl.[NH2:2][CH2:3][C:4]1[S:5][C:6]([Br:9])=[CH:7][N:8]=1.CO.C[O-].[Na+].[CH:15](O)=[O:16]>C(OCC)=O>[Br:9][C:6]1[S:5][C:4]([CH2:3][NH:2][CH:15]=[O:16])=[N:8][CH:7]=1

Komponenten

6

Reaktionsbedingungen

Temperatur
48 °C

Versuchsvorschrift

2-Aminomethyl-5-bromothiazole hydrochloride (350 g) was dissolved in 7 L of ethyl formate. To this solution were added 296 ml of a 28% methanol solution of sodium methoxide and 173 ml of a formic acid solution. The mixture was then stirred at an internal temperature of 48° C. for 5 hr. The solvent was removed by evaporation under the reduced pressure. When precipitate occurred, ethanol was added to dissolve the precipitate. The solvent was again removed by evaporation under the reduced pressure until crystal was formed. The solution was stirred under ice cooling overnight. The precipitated crystal was then collected by filtration, was then washed with cold ethanol and hexane, and was dried under the reduced pressure to give 189 g of 5-bromo-2-formylaminomethylthiazole. Further, the filtrate was concentrated, and the concentrate was crystallized from ethanol to give 58 g of secondary-crystal.

Aufarbeitung

  1. customThe solvent was removed by evaporation under the reduced pressure
  2. additionethanol was added
  3. dissolutionto dissolve the precipitate
  4. customThe solvent was again removed by evaporation under the reduced pressure until crystal
  5. customwas formed
  6. stirringThe solution was stirred under ice cooling overnight
  7. filtrationThe precipitated crystal was then collected by filtration
  8. washwas then washed with cold ethanol and hexane
  9. customwas dried under the reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-f522a6b86a614f79af3c6c32202a8df0
Quelldatensatz
uspto-grants-2009_07
Patentnummer
US07563901B2

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