HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295923Generated: October 31, 2026
Water → 5-Cyano-2-ethoxy-N,4-dimethylbenzamide
https://huagongshe.com/reaction/1295923
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 5-Bromo-2-ethoxy-N,4-dimethylbenzamide | HCID 22929845 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Propionitrile | HCID 7854 | — |
| Product | 5-Cyano-2-ethoxy-N,4-dimethylbenzamide | HCID 22929870 | 58% |
Reaction Steps
After dissolving N1,4-dimethyl-5-bromo-2-ethoxybenzamide (200 g) in propionitrile (1.51), sodium cyanide (72 g), copper iodide (14 g) and tetrakis(triphenylphosphine)palladium (42 g) were added under a nitrogen atmosphere and the mixture was heated to reflux for 5 hours. Ethyl acetate and water were added and the reaction mixture was filtered through celite. The precipitated crystals in the filtrate were filtered off (15.4 g). This filtrate was then separated and washed with brine. The organic layer was dried over anhydrous magnesium sulfate and was concentrated after filtering off the insoluble portion. The obtained crystals were filtered off and washed with ethyl acetate (77.64 g). The crystals were combined to yield the title compound (93.04 g) as a white solid.
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-98ee0fdc771c4be2b269a65bdde330ed |
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| Source note | uspto-grants-2007_07 |
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