Ethyl Acetate → 2-(4,5-Difluoro-2-nitro-phenylamino)-5-trifluoromethyl-benzonitrile

HRID 131335

Reaction equation

HRID 131335 reaction equation
F[C:2]1[CH:9]=[CH:8][C:7]([C:10]([F:13])([F:12])[F:11])=[CH:6][C:3]=1[C:4]#[N:5].[F:14][C:15]1[C:20]([F:21])=[CH:19][C:18]([NH2:22])=[C:17]([N+:23]([O-:25])=[O:24])[CH:16]=1.O.[OH-].[Li+].C(OCC)(=O)C>CS(C)=O>[F:14][C:15]1[C:20]([F:21])=[CH:19][C:18]([NH:22][C:2]2[CH:9]=[CH:8][C:7]([C:10]([F:13])([F:12])[F:11])=[CH:6][C:3]=2[C:4]#[N:5])=[C:17]([N+:23]([O-:25])=[O:24])[CH:16]=1

Participants

6

Procedure

Heat a solution of 2-fluoro-5-trifluoromethyl-benzonitrile (1.0 g, 5.74 mmol) with 4,5-difluoro-2-nitro-phenylamine (1.09 g, 5.74 mmol) and lithium hydroxide monohydrate (0.48 g, 11.49 mmol) in DMSO (12 ml) to 55° C. for 16 hours. Cool the reaction to ambient temperature and then add approximately 150 ml of ice water and stir the mixture for one hour. Extract with three 200 ml portions of dichloromethane. Combine organic layers, dry over sodium sulfate and evaporate solvent. Purify the residue via flash chromatography eluting with a linear gradient starting with 100% hexanes and going to 70% hexanes: 30% ethyl acetate to obtain 0.995 g (2.90 mmol, 50% yield) of the title compound as a yellow amorphous solid: Mass Spectrum (m/e): 344 (M+1).

Workup

  1. temperatureCool
  2. customthe reaction to ambient temperature
  3. extractionExtract with three 200 ml portions of dichloromethane
  4. dry with materialCombine organic layers, dry over sodium sulfate
  5. customevaporate solvent
  6. customPurify the residue via flash chromatography
  7. washeluting with a linear gradient

Sources & evidence

ORD record
ord-9f2ac96a8a4a4b6999fcc549bb9bedd3
Source dataset
uspto-grants-2008_06
Patent number
US07384934B2

Linked notes

Loading…