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m-Chloroperbenzoic acid → Methyl 9,10-epoxyoctadecanoate

HRID 2279684
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2279684
[C:1]([O:20][CH3:21])(=[O:19])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8]/[CH:9]=[CH:10]\[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18].ClC1C=CC=C(C(OO)=[O:30])C=1>ClCCl>[CH2:11]([CH:10]1[O:30][CH:9]1[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][C:1]([O:20][CH3:21])=[O:19])[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 70297m-Chloroperbenzoic acidHCID 5364509Methyl Oleate

Produkt 1

HCID 543923Methyl 9,10-epoxyoctadecanoate

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

Methyl oleate (1) (5.0 g; 0.017 mol) (89%) (ITERG) and meta-chloroperbenzoic acid (mCPBA) (4.3 g; 0.025 mol) (Aldrich) were dissolved in dichloromethane (J. T. Baker) (100 mL) and the reaction mixture was mixed under agitation at ambient temperature for 5 hours. The reaction mixture was then filtered and the collected solution was washed with saturated aqueous sodium bicarbonate (3×50 mL) (Aldrich) then with water (3×50 mL). The organic layer was separated and dried over anhydrous sodium sulfate. Finally, the solvent was removed by evaporation under rotation to obtain the intermediate compound 2.

Aufarbeitung

  1. additionthe reaction mixture was mixed under agitation at ambient temperature for 5 hours
  2. filtrationThe reaction mixture was then filtered
  3. washthe collected solution was washed with saturated aqueous sodium bicarbonate (3×50 mL) (Aldrich)
  4. customThe organic layer was separated
  5. dry with materialdried over anhydrous sodium sulfate
  6. customFinally, the solvent was removed by evaporation under rotation

Quellen und Nachweise

ORD-Eintrag
ord-e535bc0e18e74cdbaa96dd3b6bc4c323
Quelldatensatz
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09133305B2

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