Réaction #833526

ord-de40f9576c934f56ac948ce2cd1a2c83

Équation de réaction

CC1(COCCCCCCBr)COC1
3-[(6-bromohexyloxy)methyl]-3-methyloxetane
CCOC(=O)c1ccc(O)cc1
ethyl 4-hydroxybenzoate
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CN(C)C=O
dimethyl formamide
CCOC(=O)c1ccc(OCCCCCCOCC2COC2C)cc1
ethyl 4-[6-(2-methyloxetane-3-ylmetoxy)hexyloxy)benzoate
Rendement 80.6%

Solvants

Conditions de réaction

Température
90°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autreto terminate
  2. 2
    Autrethe reaction
  3. 3
    Extractionafter extraction with ethyl acetate
  4. 4
    Extractionthe liquid extract
  5. 5
    Lavagewas washed with an aqueous solution of 2N-sodium hydroxide and water successively
  6. 6
    Séchagethe organic layer was dried over anhydrous magnesium sulfate
  7. 7
    AutreThe residues obtained
  8. 8
    workup.DISTILLATIONby distilling off the solvent
  9. 9
    Autrewere purified on silica gel chromatography (toluene/ethyl acetate=8/2)

Mode opératoire

A mixture of 3-[(6-bromohexyloxy)methyl]-3-methyloxetane (84 g), ethyl 4-hydroxybenzoate (50 g), potassium carbonate (50 g) and dimethyl formamide (600 mL) was stirred at 90° C. for 4 hours. Water was added to the reaction mixture to terminate the reaction and, after extraction with ethyl acetate, the liquid extract was washed with an aqueous solution of 2N-sodium hydroxide and water successively, and the organic layer was dried over anhydrous magnesium sulfate. The residues obtained by distilling off the solvent were purified on silica gel chromatography (toluene/ethyl acetate=8/2), to obtain ethyl 4-[6-(2-methyloxetane-3-ylmetoxy)hexyloxy)benzoate (85 g).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07393569B2uspto-grants-2008_07