2-Butyne-1,4-diol → 4-(Tetrahydro-pyran-2-yloxy)-but-2-yn-1-ol

HRID 1496

Reaktionsgleichung

Reaktionsgleichung von HRID 1496
[CH2:1]([OH:6])[C:2]#[C:3][CH2:4][OH:5].[O:7]1[CH:12]=[CH:11][CH2:10][CH2:9][CH2:8]1>CCOCC>[O:7]1[CH2:12][CH2:11][CH2:10][CH2:9][CH:8]1[O:5][CH2:4][C:3]#[C:2][CH2:1][OH:6]

Komponenten

4

Edukt 2

HCID 80662-Butyne-1,4-diolHCID 80803,4-dihydro-2H-pyran

Produkt 1

HCID 111233154-(Tetrahydro-pyran-2-yloxy)-but-2-yn-1-olAusbeute 68,8 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 3283Diethyl EtherLösungsmittel2×

Versuchsvorschrift

To a mixture of 5.0 g of 2-butyne-1,4-diol and 10 milligrams of p-toluenesulfonic add and 150 ml of dry ether there was added dropwise with stirring at room temperature 4.9 g of 3,4-dihydro-2H-pyran. After stirring overnight at ambient temperature the ether was evaporated and the residue was poured into 200 ml of water. The aqueous solution was extracted with hexane (2×100 ml) and then re-extracted with ether (3×100 ml). The combined ether extracts were washed with 100 ml of brine, dried over magnesium sulfate and evaporated to yield 6.8 g of 4-tetrahydropyranoxy-2-butyn-1-ol.

Aufarbeitung

  1. additionof p-toluenesulfonic add
  2. customwas evaporated
  3. additionthe residue was poured into 200 ml of water
  4. extractionThe aqueous solution was extracted with hexane (2×100 ml)
  5. extractionre-extracted with ether (3×100 ml)
  6. washThe combined ether extracts were washed with 100 ml of brine
  7. dry with materialdried over magnesium sulfate
  8. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-65c75dc89f17409bb6ee8bc64675c761
Quelldatensatz
uspto-grants-1998_03
Patentnummer
US05726162

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