HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2079950Generated: October 30, 2026
Toluene → 2-Amino-6-(2-cyanoethyl)-nicotinic acid methyl ester
https://huagongshe.com/reaction/2079950
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Diethyl aluminum cyanide | HCID 16686413 | — |
| Reactant | 2-Amino-6-vinyl-nicotinic acid methyl ester | HCID 58319054 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Amino-6-(2-cyanoethyl)-nicotinic acid methyl ester | HCID 58387990 | 21% |
Reaction Steps
To a solution of 2-amino-6-vinyl-nicotinic acid methyl ester (760 mg, 4.26 mmol) in tetrahydrofuran (76 mL) was added a solution of diethyl aluminum cyanide in toluene (12.8 mL, 12.8 mmol) dropwise under sodium chloride—an ice bath cooling, at an internal temperature of −5° C. or below, then, the solution was gradually allowed to room temperature and stirred overnight. The reaction solution was partitioned into an aqueous solution of saturated ammonium chloride and ethyl acetate. This organic layer was separated, washed with brine and dried over anhydrous magnesium sulfate. The solvent was evaporated in vacuo, the residue was purified by silica gel column chromatography, and the title compound (180 mg, 0.878 mmol, 21%) was obtained as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07932272B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-1fad45fe537746ec9e4f9f66498ed0a5 |
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| Source note | uspto-grants-2011_04 |
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