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Water → HCID 14552389, Verbindung

HRID 654746
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 654746
[CH2:1]([NH:4][C@@H:5]1[CH2:14][CH2:13][C:8]2([O:12][CH2:11][CH2:10][O:9]2)[CH2:7][C@H:6]1[C:15]([O:17][CH2:18][CH3:19])=[O:16])[CH2:2][CH3:3].[C:20]([O:24][CH2:25][CH3:26])(=[O:23])[CH:21]=[CH2:22].O>C(O)C>[CH2:25]([O:24][C:20](=[O:23])[CH2:21][CH2:22][N:4]([CH2:1][CH2:2][CH3:3])[C@@H:5]1[CH2:14][CH2:13][C:8]2([O:12][CH2:11][CH2:10][O:9]2)[CH2:7][C@H:6]1[C:15]([O:17][CH2:18][CH3:19])=[O:16])[CH3:26]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 962WaterHCID 8821Ethyl Acrylate3×HCID 14552387HCID 14552387, Verbindung

Produkt 1

HCID 14552389HCID 14552389, VerbindungAusbeute 59,8 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel

Versuchsvorschrift

Ethyl 8-(propylamino)-trans-1,4-dioxaspiro -[4.5]-decane-7-carboxylate (129.6 g, 0.48 mole) was dissolved in ethanol (1500 ml), then ethyl acrylate (479 g, 4.8 mole) was added. The mixture was refluxed overnight, then additional ethyl acrylate (479 g, 4.8 mole) was added. The mixture was refluxed for 24 hours, at which time a third addition of ethyl acrylate (479 g, 0.48 mole) was made, followed by 60 hours of reflux. The mixture was then cooled to room temperature, poured into water, and the hydrogen ion concentration was adjusted to pH 10. The product was extracted with methylene chloride, dried with sodium sulfate and evaporated to give 177.4 g of crude product. This was purified by HPLC to give 102.1 g of the title product (59.8%).

Aufarbeitung

  1. temperatureThe mixture was refluxed overnight
  2. temperatureThe mixture was refluxed for 24 hours, at which time
  3. temperatureof reflux
  4. concentrationthe hydrogen ion concentration
  5. extractionThe product was extracted with methylene chloride
  6. dry with materialdried with sodium sulfate
  7. customevaporated
  8. customto give 177.4 g of crude product
  9. customThis was purified by HPLC

Quellen und Nachweise

ORD-Eintrag
ord-f60ebd9b31c54e878c95d4502a58a9e1
Quelldatensatz
uspto-grants-1992_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05134143

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