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Dimethylformamide → HCID 54363898, Verbindung

HRID 1291690
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1291690
[H-].[Na+].[CH3:3]N(C)C=O.[C:8]([O:28][CH2:29][CH3:30])(=[O:27])[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15]/[CH:16]=[CH:17]\[CH2:18][C@@H:19]([CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26])[OH:20].CI>CCCCCC>[CH3:3][O:20][CH:19]([CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26])[CH2:18][CH:17]=[CH:16][CH2:15][CH2:14][CH2:13][CH2:12][CH2:11][CH2:10][CH2:9][C:8]([O:28][CH2:29][CH3:30])=[O:27]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 6228DimethylformamideHCID 6328Methyl iodideHCID 24758Sodium hydrideHCID 6437405Ethyl Ricinoleate

Produkt 1

HCID 54363898HCID 54363898, VerbindungAusbeute 92 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8058Hexane
Lösungsmittel

Reaktionsbedingungen

Temperatur
40 °C

Versuchsvorschrift

To a 1-l flask equipped with a stirrer, a dropping funnel and a condenser, 24 g (0.6 mol) of 60% sodium hydride, 500 ml of dimethylformamide were charged, followed by the dropwise addition of a solution of 163.3 g (0.5 mol) of ethyl ricinoleate in 142 g (1.0 mol) of methyl iodide over one hour while stirring at 40° C. under an N2 atmosphere. After the completion of the dropwise addition, stirring was conducted at 40° for further 6 hours. To the reaction mixture so obtained, hexane was added. The resulting mixture was then washed with an aqueous solution of ammonium chloride and an aqueous solution of sodium thiosulfate, followed by concentration under reduced pressure. The residue was purified by chromatography on a silica gel column, whereby 155.8 g of ethyl 12-methoxy-9-octadecenoate were obtained (yield: 92%).

Aufarbeitung

  1. customTo a 1-l flask equipped with a stirrer, a dropping funnel and a condenser
  2. additionAfter the completion of the dropwise addition
  3. stirringstirring
  4. customTo the reaction mixture so obtained
  5. washThe resulting mixture was then washed with an aqueous solution of ammonium chloride
  6. concentrationan aqueous solution of sodium thiosulfate, followed by concentration under reduced pressure
  7. customThe residue was purified by chromatography on a silica gel column

Quellen und Nachweise

ORD-Eintrag
ord-4514e45603e2450eadb040dc4c4f2805
Quelldatensatz
uspto-grants-1998_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05753707

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