Reaction #2275445

Reaction equation

toluene

phenylboronic acid

Na2CO3

5-bromo-2-(3,4-dichlorophenoxy)-benzaldehyde

→

title product

3,4-Dichlorophenoxy-5-phenyl-benzaldehyde

Solvents

water

ethanol

Conditions

Workup

1. 1
   OtherUnder N2 in a 50 mL round bottomed flask fitted with a magnetic stirrer
2. 2
   Otherthe mixture was degassed with N2
3. 3
   TemperatureThe reaction was next heated
4. 4
   Temperatureto reflux for 4 hr, at which time a thin layer chromatography (tlc)
5. 5
   TemperatureAfter cooling
6. 6
   workup.ADDITIONthe mixture was diluted with 100 mL of EtOAc
7. 7
   Washwashed twice with water, twice with 2 N NaOH, twice with water and finally with saturated aqueous NaCl
8. 8
   DryingAfter drying over MgSO4
9. 9
   Otherthe solvent was removed in vacuo
10. 10
    Otherto give an oily residue, 690 mg
11. 11
    OtherThis was chromatographed on silica gel
12. 12
    Washeluting with CH2Cl2:hexane (1:1)

Procedure

Under N2 in a 50 mL round bottomed flask fitted with a magnetic stirrer were placed the following reactants in order: 15 mL of toluene, 500 mg (1.4 mmol) of 5-bromo-2-(3,4-dichlorophenoxy)-benzaldehyde (from Preparation 1), 341 mg (2.8 mmol) of phenylboronic acid (Aldrich Chem. Co.), 1.5 mL of ethanol and 774 mg (5.6 mmol) of Na2CO3 in 3 mL of water. To this was added 45 mg (0.04 mmol) of tetrakis(triphenylphosphine)palladium (0) (Aldrich Chem. Co.), and the mixture was degassed with N2. The reaction was next heated to reflux for 4 hr, at which time a thin layer chromatography (tlc), using 1:1 CH2Cl2: hexane on silica gel coated plates, showed the absence of the starting aldehyde. After cooling, the mixture was diluted with 100 mL of EtOAc, washed twice with water, twice with 2 N NaOH, twice with water and finally with saturated aqueous NaCl. After drying over MgSO4, the solvent was removed in vacuo to give an oily residue, 690 mg. This was chromatographed on silica gel, eluting with CH2Cl2:hexane (1:1) to give the title product as an oil, 462 mg.

Source