Methanol → methyl 1-hydroxy-1H-pyrazole-4-carboxylate

HRID 232017Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 232017
[OH:1][N:2]1[CH:6]=[C:5]([C:7]([OH:9])=[O:8])[CH:4]=[N:3]1.S(=O)(=O)(O)O.[CH3:15]O>>[OH:1][N:2]1[CH:6]=[C:5]([C:7]([O:9][CH3:15])=[O:8])[CH:4]=[N:3]1

Komponenten

4

Edukt 3

HCID 887MethanolHCID 1118Sulfuric AcidHCID 137994111-Hydroxypyrazole-4-carboxylic acid

Produkt 1

HCID 13823205methyl 1-hydroxy-1H-pyrazole-4-carboxylateAusbeute 91 %

Versuchsvorschrift

90 g of 1-hydroxypyrazole-4-carboxylic acid (for preparation, see corresponding German Patent Application No. P 35 32 879.7) are suspended in 500 ml of methanol, and 10 ml of concentrated sulfuric acid are added. The mixture is then refluxed for 12 hours, the methanol is distilled off under reduced pressure, the solid residue is stirred in 400 ml of water, the solution is brought to pH 3 with sodium hydroxide solution, and the product is filtered off under suction and washed with water. The mother liquor is evaporated down, and a further crystalline fraction is obtained. The combined products are dried under reduced pressure to give 91 g (91% of theory) of methyl 1-hydroxypyrazole-4-carboxylate of melting point 175°.181° C. NMR (DMSO-D6): 8.35 s [1]; 7.82 s [1]; 3.80 s [3].

Aufarbeitung

  1. temperatureThe mixture is then refluxed for 12 hours
  2. distillationthe methanol is distilled off under reduced pressure
  3. filtrationthe product is filtered off under suction
  4. washwashed with water
  5. customThe mother liquor is evaporated down
  6. customa further crystalline fraction is obtained
  7. customThe combined products are dried under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-877102d6cf1b489997739dc4a79e23ea
Quelldatensatz
uspto-grants-1989_07
Patentnummer
US04851410

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