Reaktion #564464

ord-9735ef85225047049438370d31166430

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONAfter the addition
  2. 2
    workup.DISTILLATIONthe solvent was distilled off
  3. 3
    SonstigeThe residue was purified by silica gel column chromatography

Vorschrift

16.7 g of 4-bromo-3-methylbutanol was dissolved in 200 ml of anhydrous methylene chloride, and with ice cooling, 10.0 g of dihydropyran was added dropwise. After the addition, the mixture was stirred at room temperature for 2 hours, and then the solvent was distilled off. The residue was purified by silica gel column chromatography using hexane/ethyl acetate as an eluent to give 16.2 g of 2-[4-bromo-3-methylbutoxy]-tetrahydro-2H-pyran. The NMR spectrum of this product was as follows:

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04886904uspto-grants-1989_12