HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499596Generated: October 28, 2026
Dimethylcarbamoyl Chloride → tert-Butyl (E)-3-(2-cyano-4-pyridyl)acrylate
https://huagongshe.com/reaction/499596
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylcarbamoyl Chloride | HCID 6598 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Reactant | tert-Butyl (E)-3-(4-Pyridyl)acrylate | HCID 11805847 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | tert-Butyl (E)-3-(2-cyano-4-pyridyl)acrylate | HCID 59750116 | 99% |
Reaction Steps
tert-Butyl (E)-3-(4-pyridyl)acrylate (0.88 g, 4.3 mmol) was dissolved in ethyl acetate (4 ml), and 3-chloroperbenzoic acid (ca. 77%, 0.95 g, 4.3 mmol) was added thereto. The reaction mixture was stirred at room temperature for 45 hrs and subjected to a silica gel (40 g) column chromatography. The fractions eluted with ethyl acetate-ethanol (4:1) were collected and concentrated. The residue was dissolved in nitroethane (5 ml), and trimethylsilyl cyanide (0.63 g, 6.3 mmol) and N,N-dimethylcarbamoyl chloride (0.68 g, 6.3 mmol) were added thereto. The reaction mixture was stirred at room temperature for 20 hrs and combined with ethyl acetate and water. The organic layer was successively washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated, and the residue was subjected to silica gel (30 g) column chromatography. The fractions eluted with hexane-ethyl acetate (5:1, v/v) were collected and concentrated to give the titled compound (0.73 g, 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07767665B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-351ccb9af16b4883846c827f15dfe60b |
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| Source note | uspto-grants-2010_08 |
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