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Hexane → Heptadec-2,4-dien-1-ol tetrahydropyranyl ether

HRID 622108
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 622108
[Br-].[CH2:2]([P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14].C([Li])CCC.CCCCCC.[O:45]1[CH2:50][CH2:49][CH2:48][CH2:47][CH:46]1[O:51][CH:52]1[CH2:57][CH2:56][CH2:55]CO1>O1CCCC1.CCOCC>[O:45]1[CH2:50][CH2:49][CH2:48][CH2:47][CH:46]1[O:51][CH2:52][CH:57]=[CH:56][CH:55]=[CH:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 8058HexaneHCID 263182Tetrahydropyranyl etherHCID 11124240Triphenyl(tridecyl)phosphonium bromideHCID 178418339Butyllithium

Produkt 1

HCID 56980102Heptadec-2,4-dien-1-ol tetrahydropyranyl ether

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 3283
Diethyl Ether
Lösungsmittel
HCID 8028TetrahydrofuranLösungsmittel2×

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

Tridecyltriphenyl phosphonium bromide (0.3 mole) was dissolved in 900 ml of tetrahydrofuran and cooled to 0° C. in an ice-salt bath while stirring under argon. A 2.2N solution of n-butyllithium in hexane (0.36 mole) was added dropwise over a period of 30 minutes. The mixture was stirred for an additional 20 minutes and then cooled to -70° C. in a dry ice-acetone bath. The 4-hydroxybut-2(E)-ene-1-al tetrahydropyranyl ether (0.3 mole) in 225 ml of tetrahydrofuran was added dropwise over a period of 35 minutes and the mixture stirred for an additional hour at -70° C. The mixture was then poured into 6.25 liters of ether and stirred for 20 minutes. The resulting mixture was filtered through glass fiber filter paper. The filtrate was evaporated and the residue triturated with hexane, filtered and evaporated to give a ~3:1 mixture of trans:cis isomers of the desired compound.

Aufarbeitung

  1. stirringThe mixture was stirred for an additional 20 minutes
  2. temperaturecooled to -70° C. in a dry ice-acetone bath
  3. stirringthe mixture stirred for an additional hour at -70° C
  4. stirringstirred for 20 minutes
  5. filtrationThe resulting mixture was filtered through glass fiber
  6. filtrationfilter paper
  7. customThe filtrate was evaporated
  8. customthe residue triturated with hexane
  9. filtrationfiltered
  10. customevaporated
  11. customto give
  12. additiona ~3:1 mixture of trans

Quellen und Nachweise

ORD-Eintrag
ord-fbb26e83b3cc4e7db2fa1c1d0e990b2e
Quelldatensatz
uspto-grants-1988_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04769386

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