Trifluoroacetic acid → Dipyrromethane
Reaction equation
[NH:1]1[CH:5]=[CH:4][CH:3]=[CH:2]1.[C:6](O)([C:8](F)(F)F)=O>C(OCC)(=O)C>[NH:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[CH2:3][C:2]1[NH:1][CH:5]=[CH:6][CH:8]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of p-formaldehyde (1100 mg, 35 mmol) in pyrrole (50 ml, 720 mmol), at 50° C., TFA (416 mg, 3.5 mmol) was added. The reaction mixture was kept under magnetic stirring, at room temperature, for 30 minutes, then ethyl acetate was added and the solution washed with NaHCO3 saturated solution, then the organic phase was dried on Na2SO4. After evaporation the crude product was purified by chromatography on silica gel (Petroleum Ether/Ethyl acetate 4/1+1% TEA). 1950 mg (yield 38%) of the product were obtained.
Workup
- washthe solution washed with NaHCO3 saturated solution
- customthe organic phase was dried on Na2SO4
- customAfter evaporation the crude product
- customwas purified by chromatography on silica gel (Petroleum Ether/Ethyl acetate 4/1+1% TEA)
Sources & evidence
- ORD record
- ord-6a97e73d140940c6a4a1acf3d150a40d
- Source dataset
- uspto-grants-2011_05
- Patent number
- US07947674B2
Reaction notes
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