Reaction #54957

ord-ab2ce73424b541b4a81672a916ba67f8

Reaction equation

CC(=O)Cl
acetyl chloride
COC(=O)C(C)c1ccc(OC)cc1
methyl 2-(4-methoxyphenyl)propionate
ClB(Cl)Cl
boron trichloride
COC(=O)C(C)c1ccc(O)c(C(C)=O)c1
oil
COC(=O)C(C)c1ccc(O)c(C(C)=O)c1
Methyl 2-(3-acetyl-4-hydroxyphenyl)propionate

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Temperaturecooled in an ice/salt-bath, at a rate sufficient
  2. 2
    Temperatureto maintain the temperature between -10° C. and -5° C
  3. 3
    Temperatureto maintain the temperature below 0° C
  4. 4
    workup.ADDITIONwas added
  5. 5
    workup.STIRRINGStirring
  6. 6
    workup.WAITwas continued for 1/2 hour at +3° C.
  7. 7
    workup.ADDITIONbefore pouring on
  8. 8
    Otherto crushed ice/
  9. 9
    Concentrationconcentrated hydrochloric
  10. 10
    Otherseparating the two phases
  11. 11
    ExtractionThe aqueous phase was extracted with ether (3x)
  12. 12
    Washthe combined organic extracts were washed with saturated sodium bicarbonate solution, saturated brine solution
  13. 13
    Dryingdried over anhydrous magnesium sulphate
  14. 14
    OtherEvaporation of the solvent
  15. 15
    Otheryielded the crude product as a pale yellow oil
  16. 16
    workup.DISTILLATIONVacuum distillation

Procedure

Titanium tetrachloride (82.3 mls) was added dropwise to a stirred solution of methyl 2-(4-methoxyphenyl)propionate (25 g) in dry dichloromethane (250 mls), cooled in an ice/salt-bath, at a rate sufficient to maintain the temperature between -10° C. and -5° C. The mixture was stirred for 10 minutes and acetyl chloride (10 g) was added dropwise at a rate sufficient to maintain the temperature below 0° C. The solution was stirred at -5° C. for 11/2 hours when boron trichloride (15 mls) was added. Stirring was continued for 1/2 hour at +3° C. before pouring on to crushed ice/concentrated hydrochloric and separating the two phases. The aqueous phase was extracted with ether (3x) and the combined organic extracts were washed with saturated sodium bicarbonate solution, saturated brine solution, and dried over anhydrous magnesium sulphate. Evaporation of the solvent yielded the crude product as a pale yellow oil. Vacuum distillation furnished a pale yellow oil bp 120°-125° C./0.15 mm (16.2 g; 59%)

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04151179uspto-grants-1979_04