HCID 67130964, compound → HCID 67131172, compound
Reaction equation
[C:1]([O:5][C:6]([C:8]1([O:11][C:12]2[CH:17]=[CH:16][C:15]([N+:18]([O-])=O)=[C:14]([F:21])[CH:13]=2)[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2]>[Pd].C(O)C>[C:1]([O:5][C:6]([C:8]1([O:11][C:12]2[CH:17]=[CH:16][C:15]([NH2:18])=[C:14]([F:21])[CH:13]=2)[CH2:9][CH2:10]1)=[O:7])([CH3:4])([CH3:2])[CH3:3]Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
In analogy to the procedure described in example 15.2, 1-(3-fluoro-4-nitro-phenoxy)-cyclopropanecarboxylic acid tert-butyl ester was hydrogenated in the presence of 10% palladium on charcoal in ethanol to give the title compound as brown solid. MS: m/e=268.2 [M+H+].
Sources & evidence
- ORD record
- ord-7a2e2ce94b8f4cb18ac2ce6d53869a39
- Source dataset
- uspto-grants-2011_08
- Patent number
- US08008505B2
Reaction notes
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