Water → 4-Chloro-3-methylisoxazole-5-carboxylic acid

HRID 1870495Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1870495
[Cl:1][CH:2]([C:10](=O)[CH3:11])[C:3](=[O:9])[C:4]([O:6]CC)=[O:5].Cl.[NH2:14]O.O.[OH-].[Na+]>CO>[CH3:11][C:10]1[C:2]([Cl:1])=[C:3]([C:4]([OH:6])=[O:5])[O:9][N:14]=1

Komponenten

6

Versuchsvorschrift

A solution of ethyl 3-chloro-2,4-dioxovalerate (3.0 g, 15.6 mmol) and hydroxylamine hydrochloride (1.08 g, 15.6 mmol) in a mixuture of 1.5 mL of H2O and 1 mL of CH3OH was heated to reflux. After four hours TLC analysis indicated that all of the starting material had been consumed. Sodium hydroxide (0.31 g, 7.8 mmol) was added to the hot solution. After four hours the mixture was allowed to cool to room temperature and concentrated in vacuo. The residue was taken up in a 1:1 mixture to ethyl acetate/H2O. The aqueous layer was made basic with 2N NaOH and separated. The aqueous layer was then acidified with 2M HCl and extracted with ethyl acetate (125 mL). The ethyl acetate extract was washed with H2O (2×100 mL), dried over anhydrous MgSO4, filtered and concentrated in vacuo to give 600 mg (24% yield) of the desired product a gummy tan solid: 1H NMR (CDCl3) 67 8.8 (bs, 1H), 2.3 (s, 3H).

Aufarbeitung

  1. customthat all of the starting material had been consumed
  2. waitAfter four hours the mixture was allowed
  3. concentrationconcentrated in vacuo
  4. customseparated
  5. extractionextracted with ethyl acetate (125 mL)
  6. extractionThe ethyl acetate extract
  7. washwas washed with H2O (2×100 mL)
  8. dry with materialdried over anhydrous MgSO4
  9. filtrationfiltered
  10. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-de5e1fe4ebf9485da094d24529230aae
Quelldatensatz
uspto-grants-2000_08
Patentnummer
US06096898

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