HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097518Generated: October 25, 2026
Potassium Carbonate → Methyl 2-[3-({[3-(1-cyano-1-methylethyl)phenyl]carbonyl}amino)phenoxy]-5-nitrobenzoate
https://huagongshe.com/reaction/1097518
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 2-Fluoro-5-nitrobenzoate | HCID 11217860 | — |
| Reactant | HCID 57386825 | HCID 57386825 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 2-[3-({[3-(1-cyano-1-methylethyl)phenyl]carbonyl}amino)phenoxy]-5-nitrobenzoate | HCID 66810330 | 103.3% |
Reaction Steps
To a solution of 3-(1-cyano-1-methylethyl)-N-(3-hydroxyphenyl)benzamide (5.0 g, 17.8 mmol) produced in Example 1(i) and methyl 2-fluoro-5-nitrobenzoate (3.55 g, 17.8 mmol) in N,N-dimethylformamide (50 mL) was added potassium carbonate (3.68 g, 26.7 mmol), and the mixture was stirred at room temperature for 16 hr. Insoluble material was filtered off and washed with ethyl acetate (200 mL). The filtrate and washings were combined and washed successively with 5% aqueous sodium hydrogen carbonate solution (200 mL) and saturated brine (200 mL), and dried over anhydrous sodium sulfate. Insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by basic silica gel column chromatography (eluate: ethyl acetate), and the obtained solution was concentrated under reduced pressure to give the title compound (8.45 g, 98%) as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08143258B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-8d5d709b011a475590d9bd380143f302 |
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| Source note | uspto-grants-2012_03 |
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