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Formic Acid → 5-Bromo-2-formylaminomethylthiazole

HRID 2113285
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2113285
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
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 284Formic AcidHCID 887MethanolHCID 10942334Sodium MethoxideHCID 230887761-(5-Bromo-1,3-thiazol-2-yl)methanamine hydrochloride

Produkt 1

HCID 230887625-Bromo-2-formylaminomethylthiazole

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8025Ethyl formate
Lösungsmittel

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-73cfcac6a3a143bba8746d3d3f78a58a
Quelldatensatz
uspto-grants-2009_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07524951B2

Notizen zur Reaktion

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