HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888251Generated: November 1, 2026
1-Methylnaphthalene → 2-Amino-5-cyano-N,3-dimethylbenzamide
https://huagongshe.com/reaction/888251
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Methylnaphthalene | HCID 7002 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 2-amino-5-bromo-N,3-dimethylbenzamide | HCID 44227575 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Amino-5-cyano-N,3-dimethylbenzamide | HCID 25157282 | — |
Reaction Steps
A 100-mL, three-necked flask equipped with a mechanical stirrer, thermometer and condenser was charged with 2-amino-5-bromo-N,3-dimethylbenzamide (prepared by the method of Reference Example 1) (5.0 g, 0.020 mol, 99.1% purity) and 1-methylnaphthalene (20 g) while maintaining a flow of nitrogen through a gas inlet line connected to the condenser. The reaction mixture was stirred at room temperature, and powdered sodium cyanide (powdered just prior to use) (1.25 g, 0.024 mol, assuming 95% purity), copper(I) iodide (0.57 g, 0.0030 mol) and 4-(dimethylamino)pyridine (2.10 g, 0.017 mol) were added. The mixture was heated at 160 to 165° C. for 4.25 h and then allowed to cool to 25° C. Water (20 mL) was added dropwise to the reaction mixture over 5 minutes while stirring. After stirring for an additional 30 minutes, the reaction mixture was filtered, and the solid collected was washed with water (3×10 mL) and xylenes (10 mL), and then dried to a constant weight in a vacuum-oven at 50° C. to give the title compound as a light brown solid (3.9 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08247570B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-812ba1dd127a4bbca14c717f9941bcc1 |
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| Source note | uspto-grants-2012_08 |
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