HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-Cyano-3-(ethoxycarbonylmethoxy)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | 3-(Ethoxycarbonylmethoxy)picolinamide | HCID 22038576 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Cyano-3-(ethoxycarbonylmethoxy)pyridine | HCID 22038568 | 87% |
Reaction Steps
To a solution of 3-(ethoxycarbonylmethoxy)picolinamide (5.1 g, 22.8 mmol) and triethylamine (6.68 ml, 47.9 mmol) in 100 ml of dry methylene chloride is added trifluoroacetic anhydride (6.77 ml, 47.9 mmol), dropwise, at ambient temperature under argon. After stirring for 16 hours, 100 ml of water is added. The organic phase is separated and washed with aqueous sodium hydrogen carbonate to neutral pH. After drying over sodium sulfate and evaporation, the residue is purified via flash chromatography on silica gel using a methylene chloride-ethanolic ammonia gradient (99:1 to 95:5) to give 3.90 g of 2-cyano-3-(ethoxycarbonylmethoxy)pyridine (87%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07265127B2 |
| Source dataset | uspto-grants-2007_09 |
| ORD ID | ord-9785a1b2796f4a44a592041b38a6072f |
| Source note | uspto-grants-2007_09 |