Methanol → Methyl 2,3-dichloro-6-(trifluoromethyl)benzoate

HRID 1005492Notes

Reaction equation

HRID 1005492 reaction equation
[Cl:1][C:2]1[C:10]([Cl:11])=[CH:9][CH:8]=[C:7]([C:12]([F:15])([F:14])[F:13])[C:3]=1[C:4]([OH:6])=[O:5].S(Cl)(Cl)=O.[CH3:20]O.C[O-].[Na+]>C1(C)C=CC=CC=1.N1C=CC=CC=1>[Cl:1][C:2]1[C:10]([Cl:11])=[CH:9][CH:8]=[C:7]([C:12]([F:15])([F:13])[F:14])[C:3]=1[C:4]([O:6][CH3:20])=[O:5]

Participants

7

Procedure

To a solution of 1.04 g of 2,3-dichloro-6-trifluoromethylbenzoic acid in 10 ml of toluene was added 0.71 g of thionyl chloride and 1 drop of pyridine and the mixture was heated at reflux for 3 hours. After cooling, the reaction mixture was concentrated under reduced pressure, and 2,3-dichloro-6-trifluoromethylbenzoyl chloride obtained was added to a solution which is prepared by dissolving 28% methanol solution of 0.77 g of sodium methoxide into 10 ml of methanol at a temperature of from 5 to 10° C., and the solution was stirred for 2 hours at room temperature. After condensing the reaction mixture, it was extracted with ether. The extract was washed with IN-aqueous hydrochloric acid, water and saturated saline solution in series and then dried over anhydrous magnesium sulfate. The solvent was distilled under reduced pressure, and the oily substance obtained was purified by using silica gel column chromatography to obtain 0.89 g of the title compound (nD 23.3-1.4801).

Workup

  1. temperaturethe mixture was heated
  2. temperatureat reflux for 3 hours
  3. temperatureAfter cooling
  4. concentrationthe reaction mixture was concentrated under reduced pressure, and 2,3-dichloro-6-trifluoromethylbenzoyl chloride
  5. customobtained
  6. additionwas added to a solution which
  7. customis prepared
  8. customAfter condensing the reaction mixture, it
  9. extractionwas extracted with ether
  10. washThe extract was washed with IN-aqueous hydrochloric acid, water and saturated saline solution in series
  11. dry with materialdried over anhydrous magnesium sulfate
  12. distillationThe solvent was distilled under reduced pressure
  13. customthe oily substance obtained
  14. customwas purified

Sources & evidence

ORD record
ord-44b3dc73c09d4d919b43e0a816e028de
Source dataset
uspto-grants-2000_04
Patent number
US06054605

Reaction notes

Loading…