Reaction #428441

ord-643d5afc7e544ddbb95c4377245c7d0f

Reaction equation

Cc1cc(CCl)c(O)c(-n2nc3ccc(Cl)cc3n2)c1
2-(5-Chloro-2H-benzotriazol-2-yl)-6-chloromethyl-4-methyl-phenol
CCCCC(CC)CO
2-ethylhexanol
O=C([O-])[O-].[Na+].[Na+]
Sodium carbonate
CCCCC(CC)COCc1cc(C)cc(-n2nc3ccc(Cl)cc3n2)c1O
2-(5-Chloro-benzotriazol-2-yl)-6-(2-ethylhexyloxymethyl)-4-methyl-phenol
Yield 76.2%

Solvents

Conditions

Temperature
80°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    workup.STIRRINGThe slightly yellow reaction mixture is stirred at 80° C. for 3 hours
  2. 2
    Otherevaporated to dryness
  3. 3
    workup.DISSOLUTIONThe residue is dissolved in ethyl acetate
  4. 4
    Extractionextracted with aqueous citric acid (5%) and brine
  5. 5
    DryingThe organic layer is dried over sodium sulphate
  6. 6
    Filtrationfiltered
  7. 7
    Otherevaporated to dryness
  8. 8
    OtherThe crude product is purified by column chromatography (ethyl acetate/heptane 1:12)

Procedure

2-(5-Chloro-2H-benzotriazol-2-yl)-6-chloromethyl-4-methyl-phenol (5.0 g, 16 mmol) is suspended in a mixture of 2-ethylhexanol (20.0 g, 154 mmol) and acetone (5 g) and stirred at 80° C. for 15 minutes. Sodium carbonate (3.4 g, 32 mmol) is added. The slightly yellow reaction mixture is stirred at 80° C. for 3 hours and evaporated to dryness. The residue is dissolved in ethyl acetate and extracted with aqueous citric acid (5%) and brine. The organic layer is dried over sodium sulphate, filtered and evaporated to dryness. The crude product is purified by column chromatography (ethyl acetate/heptane 1:12) to yield 4.9 g of 2-(5-Chloro-benzotriazol-2-yl)-6-(2-ethylhexyloxymethyl)-4-methyl-phenol.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08895754B2uspto-grants-2014_11