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Potassium Hydroxide → 2-Propyl-5-thiazole-acetic acid

HRID 972836
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 972836
[CH2:1]([C:4]1[S:5][C:6]([CH2:9][C:10]([O:12]CC)=[O:11])=[CH:7][N:8]=1)[CH2:2][CH3:3].[OH-].[K+]>CO>[CH2:1]([C:4]1[S:5][C:6]([CH2:9][C:10]([OH:12])=[O:11])=[CH:7][N:8]=1)[CH2:2][CH3:3]
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Komponenten

4

Edukt 2

HCID 14797Potassium HydroxideHCID 54320013Ethyl (2-propyl-1,3-thiazol-5-yl)acetate

Produkt 1

HCID 214055832-Propyl-5-thiazole-acetic acidAusbeute 67 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

A mixture of 2.13 g of ethyl 2-propyl-5-thiazole acetate, 11 ml of methanol and 1.1 ml of potassium hydroxide was stirred for 1 hour under a nitrogen atmosphere at room temperature and the methanol was distilled under reduced pressure. The residue was dissolved in 5 ml of water and 2 ml of concentrated hydrochloric acid and then 2.1 g of sodium acetate were added thereto. The mixture was extracted with methylene chloride and the organic extracts were dried and evaporated to dryness. The residue was crystallized from toluene to obtain 1.24g of 2-propyl-5-thiazole-acetic acid melting at 95° C.

Aufarbeitung

  1. distillationthe methanol was distilled under reduced pressure
  2. dissolutionThe residue was dissolved in 5 ml of water
  3. addition2 ml of concentrated hydrochloric acid and then 2.1 g of sodium acetate were added
  4. extractionThe mixture was extracted with methylene chloride
  5. customthe organic extracts were dried
  6. customevaporated to dryness
  7. customThe residue was crystallized from toluene

Quellen und Nachweise

ORD-Eintrag
ord-2648237ccd9e4539a84c3db7c59c2720
Quelldatensatz
uspto-grants-1977_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04053618

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