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Formaldehyde → 2-Ethylacrylic Acid (ethyl 2-ethylacrylate)

HRID 80294
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 80294
[C:1]([CH:6]([CH2:10][CH3:11])[C:7]([OH:9])=[O:8])([O:3]CC)=[O:2].C(N[CH2:15][CH3:16])C.[CH2:17]=O.S(=O)(=O)(O)O>>[CH2:11]([CH:10]=[C:6]([CH2:15][CH3:16])[C:7]([OH:9])=[O:8])[CH3:17].[CH2:10]([C:6](=[CH2:7])[C:1]([OH:3])=[O:2])[CH3:11]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 4

HCID 712FormaldehydeHCID 1118Sulfuric AcidHCID 8021DiethylamineHCID 108989792-(Ethoxycarbonyl)butanoic acid

Produkt 1

HCID 866430252-Ethylacrylic Acid (ethyl 2-ethylacrylate)

Versuchsvorschrift

The 2-carboethoxybutyric acid obtained in step (a) was cooled to −5° C. and diethylamine was added. A solution of formalin was added dropwise into the cooled reaction mixture which was then allowed to warm to room temperature. After stirring for 24 h the reaction mixture was warmed to 60° C. and stirred for 8 h more. The mixture consisted of two layers, which were cooled to 0° C. Concentrated sulfuric acid was added and the mixture is extracted with three 200 ml portions of diethyl ether. The ether extracts were combined, dried over magnesium sulfate and filtered. The ether was removed under reduced pressure to produce ethyl 2-ethylacrylate as a yellow oil.

Aufarbeitung

  1. temperaturewas warmed to 60° C.
  2. stirringstirred for 8 h more
  3. temperaturewere cooled to 0° C
  4. extractionthe mixture is extracted with three 200 ml portions of diethyl ether
  5. dry with materialdried over magnesium sulfate
  6. filtrationfiltered
  7. customThe ether was removed under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-1f16f26fad0d4484928dff463934d3a9
Quelldatensatz
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08846021B2

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