تفاعل #1885001

ord-eb604aee49d24263a97beb8996b045e4

معادلة التفاعل

CCCc1ccc(OB(O)O)cc1
4-propylphenylboric acid
Fc1cc(Cl)cc(Br)c1
1-bromo-3-chloro-5-fluorobenzene
O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
CCO.Cc1ccccc1.O
toluene ethanol water
CCCc1ccc(-c2cc(F)cc(Cl)c2)cc1
4-propyl-1-(3-chloro-5-fluorophenyl)benzene
المردود 97.7%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةthe mixture was refluxed for 5 hours
  2. 2
    غسيلwashed with 1N hydrochloric acid and water
  3. 3
    تجفيفThen, the resulting solution was dried over magnesium sulfate
  4. 4
    workup.DISTILLATIONdistilled under reduced pressure
  5. 5
    أخرىto remove the solvent
  6. 6
    أخرىThe residue was purified by silica-gel column chromatography with heptane as eluent
  7. 7
    أخرىdried under reduced pressure

الإجراء التجريبي

At first, 25.8 g of 4-propylphenylboric acid (S1-1), 30.0 g of 1-bromo-3-chloro-5-fluorobenzene (S1-2), 2.5 g of tetrakis(triphenylphosphine)palladium, 50.1 g of sodium carbonate and 700 ml of a mixed solvent of toluene/ethanol/water=3/3/1 (volume ratio) were added into a reactor under nitrogen atmosphere, and then the mixture was refluxed for 5 hours. Next, the reaction solution was cooled to room temperature, added with toluene and then washed with 1N hydrochloric acid and water. Then, the resulting solution was dried over magnesium sulfate and then distilled under reduced pressure to remove the solvent. The residue was purified by silica-gel column chromatography with heptane as eluent and then dried under reduced pressure to obtain 34.8 g of 4-propyl-1-(3-chloro-5-fluorophenyl)benzene (S1-3). The yield of the compound (S1-3) from (S1-1) was 97.7%.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08343595B2uspto-grants-2013_01