Trifluoroacetic acid → HCID 59556943, compound

HRID 1173579Notes

Reaction equation

HRID 1173579 reaction equation
C([O:5][CH2:6][CH:7]1[N:11]([C:12]2[CH:19]=[CH:18][C:15]([C:16]#[N:17])=[C:14]([Cl:20])[CH:13]=2)[C:10](=[O:21])[C:9]([CH3:23])([CH3:22])[C:8]1=[O:24])(C)(C)C.FC(F)(F)C(O)=O.C(=O)([O-])O.[Na+]>O>[Cl:20][C:14]1[CH:13]=[C:12]([N:11]2[CH:7]([CH2:6][OH:5])[C:8](=[O:24])[C:9]([CH3:22])([CH3:23])[C:10]2=[O:21])[CH:19]=[CH:18][C:15]=1[C:16]#[N:17]

Participants

5

Reactant 3

HCID 6422Trifluoroacetic acidHCID 516892Sodium BicarbonateHCID 59556946HCID 59556946, compound

Product 1

HCID 59556943HCID 59556943, compoundYield 87%

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

To 4-[5-(tert-butoxy methyl)-3,3-dimethyl-2,4-dioxopyrrolidin-1-yl]-2-chlorobenzonitrile (900 mg) was added trifluoroacetic acid (10 mL) at 0° C., and the mixture was stirred at room temperature for 1 hr. The reaction mixture was cooled to 0° C., and neutralized with saturated sodium hydrogen carbonate solution. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=4:1→1:4), and recrystallized from hexane-ethyl acetate to give the title compound as colorless crystals (yield: 655 mg, 87%).

Workup

  1. temperatureThe reaction mixture was cooled to 0° C.
  2. extractionthe mixture was extracted with ethyl acetate
  3. washThe extract was washed with saturated brine
  4. dry with materialdried over anhydrous magnesium sulfate
  5. concentrationconcentrated under reduced pressure
  6. customThe residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=4:1→1:4)
  7. customrecrystallized from hexane-ethyl acetate

Sources & evidence

ORD record
ord-0ad52e65032a4a32873e398770116fb3
Source dataset
uspto-grants-2010_11
Patent number
US07834051B2

Reaction notes

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