Réaction #631994

ord-c033d13ee9a64d279fa17ee08eea6686

Équation de réaction

CCOC(C)OC1CCC(C)(C)CC1C(=O)OC
2-carbomethoxy-4,4-dimethyl-1-(2-methyl-1,3-dioxapent-1-yl)cyclohexane
C=[CH][Mg][Br]
vinylmagnesium bromide
C=CBr
vinyl bromide
Cl
HCl
C=CCCC(=O)C1CC(C)(C)CCC1O
1-(2-hydroxy-5,5-dimethyl-1-cyclohexyl)-4-penten-1-one
Rendement 60.0%

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    TempératureAfter 4 hours the mixture was cooled
  2. 2
    ExtractionExtraction of the mixture
  3. 3
    Autrewith Et2O, removal of the solvents

Mode opératoire

A solution of 2-carbomethoxy-4,4-dimethyl-1-(2-methyl-1,3-dioxapent-1-yl)cyclohexane (5.16 g) in 10 ml of THF was added dropwise, over 15 minutes, to a solution of vinylmagnesium bromide (1.2 g) and vinyl bromide (5.35 g) in 20 ml of THF at 65° C. After 4 hours the mixture was cooled and poured into cold 20% aqueous HCl (40 ml). Extraction of the mixture with Et2O, removal of the solvents and a SiO2 chromatography (CH2Cl2/AcOEt) provide pure 1-(2-hydroxy-5,5-dimethyl-1-cyclohexyl)-4-penten-1-one (yield 60%).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07935669B2uspto-grants-2011_05