HCID 20081816, compound → HCID 9878343, compound
Reaction equation
[CH3:1][C:2]1[NH:3][C:4]([CH3:19])=[CH:5][CH:6]([C:12]2[CH:17]=[CH:16][C:15]([F:18])=[CH:14][CH:13]=2)[C:7]=1[C:8]([O:10][CH3:11])=[O:9]>C(O)(=O)C.[O-2].[Cr+6].[O-2].[O-2]>[CH3:1][C:2]1[C:7]([C:8]([O:10][CH3:11])=[O:9])=[C:6]([C:12]2[CH:17]=[CH:16][C:15]([F:18])=[CH:14][CH:13]=2)[CH:5]=[C:4]([CH3:19])[N:3]=1Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
8.6g (33 mmol) of crude product from Example 27 and 3.3 g of chromium(VI) oxide are heated under reflux for 1 hour in 90 ml of glacial acetic acid. The solvent is then removed on the rotary evaporator, ethyl acetate/petroleum ether 1:1 is added to the residue and undissolved material is filtered off with suction. The mother liquor is concentrated in vacuo and chromatographed over 500 g of silica gel using ethyl acetate/petroleum ether 1:1.
Workup
- customThe solvent is then removed on the rotary evaporator, ethyl acetate/petroleum ether 1:1
- additionis added to the residue and undissolved material
- filtrationis filtered off with suction
- concentrationThe mother liquor is concentrated in vacuo
- customchromatographed over 500 g of silica gel
Sources & evidence
- ORD record
- ord-1c25c2e1c4df46388ca5995699970717
- Source dataset
- uspto-grants-1995_03
- Patent number
- US05401746
Reaction notes
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