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Ammonium Chloride → Ethyl 8-acetyl-12-(acetyloxy)-8-methylheptadecanoate

HRID 1439489
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1439489
[I-].[CH3:2][Li].[C:4]([C:7](Br)([CH2:19][CH2:20][CH2:21][CH:22]([O:28][C:29](=[O:31])[CH3:30])[CH2:23][CH2:24][CH2:25][CH2:26][CH3:27])[CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][C:14]([O:16][CH2:17][CH3:18])=[O:15])(=[O:6])[CH3:5].[Cl-].[NH4+]>CCOCC>[C:4]([C:7]([CH3:2])([CH2:19][CH2:20][CH2:21][CH:22]([O:28][C:29](=[O:31])[CH3:30])[CH2:23][CH2:24][CH2:25][CH2:26][CH3:27])[CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][C:14]([O:16][CH2:17][CH3:18])=[O:15])(=[O:6])[CH3:5]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 25517Ammonium ChlorideHCID 30165Iodide IonHCID 21397377Ethyl 8-acetyl-12-(acetyloxy)-8-bromoheptadecanoateHCID 178418348HCID 178418348, Verbindung

Produkt 1

HCID 21397375Ethyl 8-acetyl-12-(acetyloxy)-8-methylheptadecanoate

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 3283
Diethyl Ether
Lösungsmittel
2×

Versuchsvorschrift

Cupruous iodide (7.1 g., 0.037 mole) is suspended in ether (150 ml.) and a 1.66 M solution of methyl lithium in ether (45 ml., 0.075 mole) is added dropwise during 30 minutes. Ethyl 8-acetyl-8-bromo-12-acetoxyheptadecanoate (11.9 g., 0.025 mole) is added dropwise during 30 minutes. The temperature is kept at -4° C to -2° C. during these operations by means of a salt bath. Stirring is continued at this temperature for another 30 minutes; then the mixture is stirred for 2 hours without cooling. The reaction mixture is then treated with 200 ml. of saturated ammonium chloride solution. the organic layer is separated, washed with brine and dried over sodium sulfate. Distillation of the solvent in vacuo leaves the crude product as an orange oil weighing 9.2 g. The product is purified by column chromatography using 250 g. of silica gel and chloroform as the eluant. Ethyl 8-acetyl-8-methyl-12-acetoxyheptadecanoate is obtained as yellow viscous oil.

Aufarbeitung

  1. customThe temperature is kept at -4° C to -2° C. during these operations by means of a salt bath
  2. stirringthen the mixture is stirred for 2 hours
  3. temperaturewithout cooling
  4. additionThe reaction mixture is then treated with 200 ml
  5. customthe organic layer is separated
  6. washwashed with brine
  7. dry with materialdried over sodium sulfate
  8. distillationDistillation of the solvent in vacuo
  9. customleaves the crude product as an orange oil
  10. customThe product is purified by column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-ff11ab0cca9e44f69ea808472b50fb0c
Quelldatensatz
uspto-grants-1977_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04059602

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