Réaction #1483059

ord-d1c73ab6e7074e48b13b11e620cbccc0

Équation de réaction

OCC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)CO
2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9-hexadecafluorodecane-1,10-diol
[K+].[OH-]
potassium hydroxide
BrCc1ccccc1
benzyl bromide
OCC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)COCc1ccccc1
10-(benzyloxy)-2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9-hexadecafluorodecan-1-ol

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.ADDITIONwas added dropwise over 15 minutes
  2. 2
    ConcentrationThe reaction mixture was concentrated in vacuo
  3. 3
    Autrethe residue was partitioned between aqueous saturated ammonium chloride and ethyl acetate
  4. 4
    ExtractionThe aqueous layer was extracted twice with EtOAc
  5. 5
    Lavagewashed with water
  6. 6
    Séchagebrine, dried over MgSO4
  7. 7
    Concentrationconcentrated in vacuo
  8. 8
    AutreThe residue was purified via flash column chromatography on silica gel using 5% EtOAc in petroleum ether as the eluent
  9. 9
    AutreThe product was isolated as colorless oil
  10. 10
    Autreupon drying under high vacuum for 12 h

Mode opératoire

A dry 5 mL round bottom flask was charged with 2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9-hexadecafluorodecane-1,10-diol (2.2 mmol, 1.0 g), dry DMF (2.5 mL), and crushed potassium hydroxide (2.2 mmol, 121 mg). The mixture was flushed with argon and benzyl bromide (0.7 mmol, 123 mg) was added dropwise over 15 minutes. The solution was allowed to stir overnight at room temperature under argon. The reaction mixture was concentrated in vacuo, and the residue was partitioned between aqueous saturated ammonium chloride and ethyl acetate. The aqueous layer was extracted twice with EtOAc. The organic layers were combined, washed with water then brine, dried over MgSO4, and concentrated in vacuo. The residue was purified via flash column chromatography on silica gel using 5% EtOAc in petroleum ether as the eluent. The product was isolated as colorless oil; upon drying under high vacuum for 12 h, the oil solidified (90%). 1H NMR (CDCl3): δ7.36 (m, 5H), 4.68 (s, 2H), 4.10 (td, 2H, J=14, 6), 3.94 (t, 2H, J=14), 1.96 (t, 1H, J=7); 13C NMR (CDCl3): δ136.6, 128.8, 128.5, 128.0, 74.7, 66.9, 60.9; 19F NMR (CDCl3): δ −119.8, −122.3, −122.8, −123.7, −123.9.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08900562B2uspto-grants-2014_12