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Hydrochloric Acid → Ethyl 2,3-dihydro-3-oxo-1H-pyrazole-4-carboxylate

HRID 1697459
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1697459
[O-]CC.[Na+].C([O:7][CH:8]=[C:9]([C:15](OCC)=O)[C:10]([O:12][CH2:13][CH3:14])=[O:11])C.O.[NH2:21][NH2:22].Cl>C(O)C.O>[CH2:13]([O:12][C:10]([C:9]1[C:8](=[O:7])[NH:21][NH:22][CH:15]=1)=[O:11])[CH3:14]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 313Hydrochloric AcidHCID 6871Diethyl (ethoxymethylene)malonateHCID 24654Hydrazine hydrate (1:1)HCID 2723922Sodium ethoxide

Produkt 1

HCID 238933Ethyl 2,3-dihydro-3-oxo-1H-pyrazole-4-carboxylateAusbeute 84,5 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 702
Ethanol
Lösungsmittel
HCID 962WaterLösungsmittel

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

To a solution of sodium ethoxide (20.8 g, 0.31 mol) and diethyl ethoxymethylenemalonate (20 mL, 0.10 mol) in ethanol (400 mL), was added hydrazine monohydrate (10.0 mL, 0.20 mol) with cooling in an ice-cold water bath. The mixture was then heated at 80° C. for 3 h. The resulting mixture was diluted with water (200 mL) and neutralized with 10M HCl solution until pH 6. The mixture was extracted several times with chloroform. The aqueous layer was acidified to pH 2 and extracted again with chloroform. The combined organic layers were dried (Na2SO4) and concentrated to a solid which was washed with methanol and ether and dried to give the product (13.2 g, 80%) as a solid. 1H NMR (400 MHz, DMSO-d6) δ7.89 (s, 1H), 4.15 (q, 211, J=7.12 Hz), 1.23 (t, 3H, J=7.11 Hz).

Aufarbeitung

  1. temperaturewith cooling in an ice-cold water bath
  2. extractionThe mixture was extracted several times with chloroform
  3. extractionextracted again with chloroform
  4. dry with materialThe combined organic layers were dried (Na2SO4)
  5. concentrationconcentrated to a solid which
  6. washwas washed with methanol and ether
  7. customdried

Quellen und Nachweise

ORD-Eintrag
ord-9c6aeca92955443a8f250568a8ec23b4
Quelldatensatz
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08163901B2

Notizen zur Reaktion

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