Tetrahydrofuran → HCID 59191291, compound
Reaction equation
[CH2:1]([C:3]1[CH:8]=[CH:7][C:6]([O:9][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=2[N+:16]([O-])=O)=[C:5]([O:19][CH3:20])[CH:4]=1)[CH3:2].C1COCC1>C(O)C>[CH2:1]([C:3]1[CH:8]=[CH:7][C:6]([O:9][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=2[NH2:16])=[C:5]([O:19][CH3:20])[CH:4]=1)[CH3:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
According to the procedure of example 20(b) except substituting 4-ethyl-2-methoxy-1-[4-nitro-2-(trifluoromethyl)phenoxy]benzene by 4-ethyl-2-methoxy-1-(2-nitrophenoxy)benzene (0.66 mmol; 180 mg) and THF by ethanol, the title compound was prepared in quantitative yield (181 mg) and used without further purification.
Workup
- customused without further purification
Sources & evidence
- ORD record
- ord-3a26f309d76d4d149cbfeb4306ebfeb2
- Source dataset
- uspto-grants-2014_05
- Patent number
- US08722746B2
Reaction notes
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