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Hydrazine → Oxane-4-carbohydrazide

HRID 710943
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 710943
[O:1]1[CH2:6][CH2:5][CH:4]([C:7]([O:9]C)=O)[CH2:3][CH2:2]1.[NH2:11][NH2:12]>CO>[O:1]1[CH2:6][CH2:5][CH:4]([C:7]([NH:11][NH2:12])=[O:9])[CH2:3][CH2:2]1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 9321HydrazineHCID 27735202H-Pyran-4-carboxylic acid, tetrahydro-, methyl ester

Produkt 1

HCID 28064717Oxane-4-carbohydrazideAusbeute 66,1 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

A solution of methyl tetrahydro-2H-pyran-4-carboxylate (1.44 g, 10.0 mmol) in methanol (50 mL) was stirred at 50° C. To the reaction mixture, hydrazine.monohydrate (0.675 g) was added, followed by stirring at the same temperature for 2 hours, after completion of the reaction, the reaction mixture was concentrated and diluted with methylene chloride, the solution was then washed with saturated sodium bicarbonate aqueous solution and saturated brine, and the organic layer was dried over magnesium sulfate and the solvent was distilled off under reduced pressure to afford 952 mg of the title compound (yield 66.1%).

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Aufarbeitung

  1. customafter completion of the reaction
  2. concentrationthe reaction mixture was concentrated
  3. additiondiluted with methylene chloride
  4. washthe solution was then washed with saturated sodium bicarbonate aqueous solution and saturated brine
  5. dry with materialthe organic layer was dried over magnesium sulfate
  6. distillationthe solvent was distilled off under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-07c71cfcc2b64bec8a6a927da5a832e3
Quelldatensatz
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09181250B2

Notizen zur Reaktion

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