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Water → HCID 86665236, Verbindung

HRID 1053544
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1053544
[CH2:1]([OH:21])[CH2:2][CH2:3][CH2:4]/[CH:5]=[CH:6]\[CH2:7]/[CH:8]=[CH:9]\[CH2:10]/[CH:11]=[CH:12]\[CH2:13]/[CH:14]=[CH:15]\[CH2:16]/[CH:17]=[CH:18]\[CH2:19][CH3:20].[C:22]([O:27]Br)(=[O:26])[CH:23]([CH3:25])[CH3:24].[OH-].[Na+].O>[Cl-].C([N+](CCCC)(CCCC)CCCC)CCC.C1(C)C=CC=CC=1>[CH2:1]([O:21][C:23]([CH3:25])([CH3:24])[C:22]([O:27][C:23]([CH3:25])([CH3:24])[CH3:22])=[O:26])[CH2:2][CH2:3][CH2:4]/[CH:5]=[CH:6]\[CH2:7]/[CH:8]=[CH:9]\[CH2:10]/[CH:11]=[CH:12]\[CH2:13]/[CH:14]=[CH:15]\[CH2:16]/[CH:17]=[CH:18]\[CH2:19][CH3:20]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 962WaterHCID 14798Sodium HydroxideHCID 21270289HCID 21270289, VerbindungHCID 59539494(5Z,8Z,11Z,14Z,17Z)-icosa-5,8,11,14,17-pentaen-1-ol

Produkt 1

HCID 86665236HCID 86665236, VerbindungAusbeute 44,4 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 70681
Tetrabutylammonium Chloride
Katalysator
HCID 1140TolueneLösungsmittel

Versuchsvorschrift

A mixture of (5Z,8Z,11Z,14Z,17Z)-icosa-5,8,11,14,17-pentaen-1-ol, (0.83 g, 3.14 mmol), tetrabutylammonium chloride (0.24 g, 0.85 mmol) and t-butyl □-bromo isobutyrate (3.50 g, 15.7 mmol) was dissolved in toluene (15 mL) and placed under nitrogen. An aqueous solution of sodium hydroxide (50%, 5 mL) was added slowly under vigorous stirring at room temperature. The resulting mixture was heated to 60° C. and stirred for six hours. The mixture was cooled, added water and extracted three times with ether. The combined organic extract was washed with brine, dried (Na2SO4), filtered and concentrated. The residue was purified by flash chromatography on silica gel using a gradient of 5-10% ethyl acetate in heptane as eluent. Concentration of the appropriate fractions afforded 0.60 g (44% yield) of the title compound as an oil. MS (electro spray): 453.3 [M+Na]+.

Aufarbeitung

  1. temperatureThe resulting mixture was heated to 60° C.
  2. stirringstirred for six hours
  3. temperatureThe mixture was cooled
  4. extractionextracted three times with ether
  5. extractionThe combined organic extract
  6. washwas washed with brine
  7. dry with materialdried (Na2SO4)
  8. filtrationfiltered
  9. concentrationconcentrated
  10. customThe residue was purified by flash chromatography on silica gel using a gradient of 5-10% ethyl acetate in heptane as eluent

Quellen und Nachweise

ORD-Eintrag
ord-7a41632dda4040be81151dc73bdba513
Quelldatensatz
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09394228B2

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