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Hydrochloric Acid → (2E)-4-(Dimethylamino)-2-butenoic acid hydrochloride

HRID 38505
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 38505
[CH3:1][N:2]([CH3:10])[CH2:3]/[CH:4]=[CH:5]/[C:6]([O:8]C)=[O:7].[OH-].[Na+].[ClH:13]>CO.O>[ClH:13].[CH3:1][N:2]([CH3:10])[CH2:3]/[CH:4]=[CH:5]/[C:6]([OH:8])=[O:7]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 15870798(E)-methyl 4-(dimethylamino)but-2-enoate

Produkt 1

HCID 45358758(2E)-4-(Dimethylamino)-2-butenoic acid hydrochlorideAusbeute 51 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 887MethanolLösungsmittel
HCID 962
Water
Lösungsmittel

Reaktionsbedingungen

Temperatur
50 °C

Versuchsvorschrift

Methyl (2E)-4-(dimethylamino)but-2-enoate (3.4 g, 23.7 mmol) was dissolved in methanol (25 mL). A solution of sodium hydroxide (0.95 g, 23.7 mmol) in water (7 mL) was added, and the mixture was heated to 50° C. for 1 h. The pH was then adjusted to 2 with conc. hydrochloric acid. The solution was concentrated to dryness, and the residue was triturated with ethanol (30 mL). It was filtered, and the solution was concentrated in vacuo. The residue was triturated with 2-propanol, and the precipitate was collected by suction filtration and dried to yield 2.00 g (51%) of the title compound.

Aufarbeitung

  1. concentrationThe solution was concentrated to dryness
  2. customthe residue was triturated with ethanol (30 mL)
  3. filtrationIt was filtered
  4. concentrationthe solution was concentrated in vacuo
  5. customThe residue was triturated with 2-propanol
  6. filtrationthe precipitate was collected by suction filtration
  7. customdried

Quellen und Nachweise

ORD-Eintrag
ord-8dd1568111f34f96ba6ac11b4e5efd23
Quelldatensatz
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08524722B2

Notizen zur Reaktion

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