Triethylamine → HCID 66940621, compound
Reaction equation
[CH3:1][O:2][C:3](=[O:15])[C:4]1[CH:9]=[C:8](F)[CH:7]=[C:6]([NH2:11])[C:5]=1[N+:12]([O-:14])=[O:13].[CH2:16](N(CC)CC)C.[CH3:23][CH2:24][O-:25].[Na+]>C(O)C>[CH2:1]([O:2][C:3](=[O:15])[C:4]1[CH:9]=[C:8]([O:25][CH2:24][CH3:23])[CH:7]=[C:6]([NH2:11])[C:5]=1[N+:12]([O-:14])=[O:13])[CH3:16]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 60 °C
Procedure
5.0 g (23.3 mmol) of 3-amino-5-fluoro-2-nitro-benzoic acid methyl ester was dissolved in ethanol and treated with 2.6 g (25.6 mmol) of triethylamine and 1.8 g (25.6 mmol) of NaOEt. The reaction was heated at 60° C. for 0.5 h to produce 3-amino-5-ethoxy-2-nitro-benzoic acid ethyl ester. LCMS: 255 (M+1)+.
Sources & evidence
- ORD record
- ord-eeb5dd96b3554c5e820db47dc864b546
- Source dataset
- uspto-grants-2015_02
- Patent number
- US08946259B2
Reaction notes
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