Tetrahydrofuran → HCID 59191322, compound
Reaction equation
[F:1][C:2]1[C:3]([CH:20]=[CH2:21])=[CH:4][C:5]([O:18][CH3:19])=[C:6]([CH:17]=1)[O:7][C:8]1[C:9]([N+:14]([O-])=O)=[N:10][CH:11]=[CH:12][CH:13]=1.C1COCC1>CO>[CH2:20]([C:3]1[C:2]([F:1])=[CH:17][C:6]([O:7][C:8]2[C:9]([NH2:14])=[N:10][CH:11]=[CH:12][CH:13]=2)=[C:5]([O:18][CH3:19])[CH:4]=1)[CH3:21]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 3-(5-fluoro-2-methoxy-4-vinylphenoxy)-2-nitropyridine (3.7 mmol, 1.1 g) and THF by methanol, the title compound was prepared as a white solid (800 mg; 80.5%) and used without further purification.
Workup
- customused without further purification
Sources & evidence
- ORD record
- ord-263b2f6b0dc94e0586903a435ba303df
- Source dataset
- uspto-grants-2014_05
- Patent number
- US08722746B2
Reaction notes
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