تفاعل #2028902

ord-ff00ac905d7943bcaa639a49024ff2da

معادلة التفاعل

C1CCOC1
THF
CCOc1ccc(-c2cccc(F)c2F)c(F)c1F
4-ethoxy-2,2′,3,3′-tetrafluorobiphenyl
[Li][CH](C)CC
sec-butyllithium
CCOC1(C=O)C=CC(c2cccc(F)c2F)=C(F)C1F
4-ethoxy-2,2′,3,3′-tetrafluorobiphenyl-4-carboaldehyde
المردود 70.0%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
-65°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىprepared by means of a conventional coupling reaction in a reaction vessel under an atmosphere of nitrogen
  2. 2
    درجة الحرارةthe reaction mixture was warmed slowly to room temperature
  3. 3
    أخرىThe reaction mixture was quenched with a saturated aqueous solution of ammonium chloride, and water (500 ml)
  4. 4
    workup.ADDITIONwas added
  5. 5
    أخرىto give two layers
  6. 6
    استخلاصThe water layer was extracted with toluene (200 ml) twice
  7. 7
    غسيلthe combined organic layer was washed with water
  8. 8
    تجفيفdried over anhydrous magnesium sulfate
  9. 9
    workup.DISTILLATIONThe solvent was distilled off under reduced pressure
  10. 10
    workup.ADDITIONThe residue was treated with silica gel chromatography (silica gel: 30 g, eluent: toluene)

الإجراء التجريبي

THF (400 ml) was added to 4-ethoxy-2,2′,3,3′-tetrafluorobiphenyl (6) (39.25 g) prepared by means of a conventional coupling reaction in a reaction vessel under an atmosphere of nitrogen. The solution was cooled to −65° C. or lower, and sec-butyllithium (1.08 M in cyclohexane and n-hexane; 141.3 ml) was added dropwise. After the reaction mixture had been stirred at −65° C. for another 1 hour, N,N,-dimethylformamide (21.2 g) was added dropwise, and the reaction mixture was warmed slowly to room temperature. The reaction mixture was quenched with a saturated aqueous solution of ammonium chloride, and water (500 ml) was added to give two layers. The water layer was extracted with toluene (200 ml) twice, and the combined organic layer was washed with water and then dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure. The residue was treated with silica gel chromatography (silica gel: 30 g, eluent: toluene) to give 4-ethoxy-2,2′,3,3′-tetrafluorobiphenyl-4-carboaldehyde (7) (30 g) in 70% yield.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08389073B2uspto-grants-2013_03