HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295970Generated: October 30, 2026
Ethyl Acetate → [5-Acetyl-3-(tert-butyl)-2-methoxyanilino]methyl cyanide
https://huagongshe.com/reaction/1295970
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Bromoacetonitrile | HCID 11534 | — |
| Reactant | HCID 22929815 | HCID 22929815 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | [5-Acetyl-3-(tert-butyl)-2-methoxyanilino]methyl cyanide | HCID 22930120 | — |
Reaction Steps
Bromoacetonitrile (6 ml) and potassium carbonate (1.4 g) were added to a solution of 1-[3-amino-5-(tert-butyl)-4-methoxyphenyl]-1-ethanone (2.0 g, 9.0 mmol) in dimethylformamide (50 ml) and the mixture was stirred at 70° C. for 3 hours. The reaction mixture was cooled to room temperature, ethyl acetate was added, washed was performed with water and brine in that order, the organic layer was dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (solvent: n-hexane-ethyl acetate) to yield the title compound (3.2 g) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07244730B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-c8d4d4db58d648f1beba4163cba6303f |
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| Source note | uspto-grants-2007_07 |
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