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Hydrochloric Acid → 2-Methoxyimino-3,3-ethylenedioxybutyric acid

HRID 463378
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 463378
[CH3:1][O:2][N:3]=[C:4]([C:10]1([O:15][CH2:14][CH2:13][O:12]1)[CH3:11])[C:5]([O:7]CC)=[O:6].[OH-].[Na+].Cl>C(O)C>[CH3:1][O:2][N:3]=[C:4]([C:10]1([O:12][CH2:13][CH2:14][O:15]1)[CH3:11])[C:5]([OH:7])=[O:6]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 54382027Ethyl 2-methoxyimino-3,3-ethylenedioxybutyrate

Produkt 1

HCID 544524052-Methoxyimino-3,3-ethylenedioxybutyric acidAusbeute 99,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel2×

Versuchsvorschrift

To a solution of ethyl 2-methoxyimino-3,3-ethylenedioxybutyrate (syn isomer, 180 g) in ethanol (1080 ml) was added 1N aqueous solution of sodium hydroxide (1660 ml) and the mixture was stirred for 2 hours and 10 minutes at ambient temperature. After the reaction mixture was adjusted to pH 7.3 with 6N hydrochloric acid, ethanol was distilled off under reduced pressure and then washed with diethyl ether (500 ml×2). To the resultant was added diethyl ether (1 l), adjusted to pH 1.5 with 6N hydrochloric acid and then diethyl ether layer was separated. The remaining aqueous layer was further extracted with diethyl ether (350 ml), and the remaining aqueous layer was adjusted to pH 1.3 with 6N hydrochloric acid and then further extracted with diethyl ether (350 ml×2). The diethyl ether layer and extracts were combined together, washed with a saturated aqueous solution of sodium chloride, dried over magnesium sulfate and then filtered. The filtrate was concentrated to give an oil (155.6 g) of 2-methoxyimino-3,3-ethylenedioxybutyric acid (syn isomer). (Yield: 99.3%)

Aufarbeitung

  1. distillationwas distilled off under reduced pressure
  2. washwashed with diethyl ether (500 ml×2)
  3. additionTo the resultant was added diethyl ether (1 l)
  4. customdiethyl ether layer was separated
  5. extractionThe remaining aqueous layer was further extracted with diethyl ether (350 ml)
  6. extractionfurther extracted with diethyl ether (350 ml×2)
  7. washwashed with a saturated aqueous solution of sodium chloride
  8. dry with materialdried over magnesium sulfate
  9. filtrationfiltered
  10. concentrationThe filtrate was concentrated

Quellen und Nachweise

ORD-Eintrag
ord-3ad2ccff251b4f26a5fd2bb7e2688b90
Quelldatensatz
uspto-grants-1985_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04518774

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