Reaktion #62706

ord-d179930b3754451789634e378a8dd266

Reaktionsgleichung

CC(C)(C)C=O
2,2-dimethylpropanal
OCC=CCO
but-2-ene-1,4-diol
O
water
CC(C)(C)C1OCC=CCO1
2-tert-butyl-4,7-dihydro-1,3-dioxepin
Ausbeute 89.9%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturwas refluxed
  2. 2
    Sonstigeformed
  3. 3
    Sonstigewas removed in the course of 3 hours (h)
  4. 4
    workup.WAITThe mixture was then left
  5. 5
    workup.ADDITION10 ml of a 25% strength sodium hydroxide solution were added to the solution
  6. 6
    Waschenthe mixture was washed neutral with a little water
  7. 7
    workup.DISTILLATIONthe toluene was distilled off under reduced pressure at from 50° to 60° C
  8. 8
    SonstigeThe residue obtained
  9. 9
    workup.DISTILLATIONwas distilled under 0.1 mbar

Vorschrift

A mixture of 430 g (5 moles) of 2,2-dimethylpropanal, 3 g of p-toluenesulfonic acid and 440 g (5 moles) of but-2-ene-1,4-diol in 1000 ml of toluene was refluxed, and the water of reaction formed was removed in the course of 3 hours (h). The mixture was then left to cool to room temperature, 10 ml of a 25% strength sodium hydroxide solution were added to the solution, the mixture was washed neutral with a little water and the toluene was distilled off under reduced pressure at from 50° to 60° C. The residue obtained was distilled under 0.1 mbar to give 702 g of 2-tert-butyl-4,7-dihydro-1,3-dioxepin of boiling point 80° C./32 mbar.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04761489uspto-grants-1988_08