تفاعل #76392

ord-3a1fee962f1a4994bba748423edf0c07

معادلة التفاعل

Oc1ccc(Br)cc1
4-bromophenol
CC1(OCCCCC(F)(F)C(F)(F)C(F)(F)C(F)(F)F)C=CC(S(=O)(=O)[O-])=CC1
4-(5,5,6,6,7,7,8,8,8-nonafluoro-octyloxy)-osylate
CC1(OCCCCC(F)(F)C(F)(F)C(F)(F)C(F)(F)F)C=CC(S(=O)(=O)[O-])=CC1
4-(5,5,6,6,7,7,8,8,8-nonafluoro-octyloxy)-tosylate
FC(F)(F)C(F)(F)C(F)(F)C(F)(F)CCCCOc1ccc(Br)cc1
1-Bromo-4-(5,5,6,6,7,7,8,8,8-nonafluoro-octyloxy)-benzene

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىquenched with water
  2. 2
    استخلاصextracted with ethyl acetate:hexane(1:1)
  3. 3
    غسيلwashed with brine
  4. 4
    تجفيفdried over MgSO4
  5. 5
    تركيزconcentrated in vacuo
  6. 6
    أخرىPurification by chromatography on silica gel (5% EtOAc/hexanes) eafforded 1-bromo-4-(5,5,6,6,7,7,8,8,8-nonafluoro-octyloxy)-benzene (47) a colorless oil (65%)

الإجراء التجريبي

To a solution of commercially available 4-bromophenol (46) (1 equi.) and 4-(5,5,6,6,7,7,8,8,8-nonafluoro-octyloxy)-osylate (10) (1 equi.) in DMF (3 mL/mmole), cesium carbonate (1.25 equi.) was added at room temperature. The reaction mixture was stirred at that temperature for 24 h, quenched with water, extracted with ethyl acetate:hexane(1:1), washed with brine, dried over MgSO4, and concentrated in vacuo. Purification by chromatography on silica gel (5% EtOAc/hexanes) eafforded 1-bromo-4-(5,5,6,6,7,7,8,8,8-nonafluoro-octyloxy)-benzene (47) a colorless oil (65%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06703082B1uspto-grants-2004_03