HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 2-Amino-4-methylpyridine-3-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 1,1-Dicyano-4,4-diethoxy-3-methyl-1-butene | HCID 19707209 | — |
| Reactant | 1,1-Dicyano-4-ethoxy-3-methyl-1,3-butadiene | HCID 54261024 | — |
| Product | 2-Amino-4-methylpyridine-3-carbonitrile | HCID 10396887 | — |
Reaction Steps
A solution of about 6.1 grams (0.038 mole) of a mixture of 1,1-dicyano-4-ethoxy-3-methyl-1,3-butadiene and 1,1-dicyano-4,4-diethoxy-3-methyl-1-butene in 200 mL of saturated methanolic ammonia is stirred at ambient temperature for about 15 hours. After this time the solvent is removed under reduced pressure, and the residue is partitioned between 160 mL of aqueous 1N hydrochloric acid and 160 mL of ethyl acetate. The aqueous layer is separated and poured into 160 mL of an aqueous solution saturated with sodium bicarbonate. The resultant solid is collected by filtration and dried, yielding about 2.6 grams of 2-amino-3-cyano-4-methylpyridine. Steps A and B are repeated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05593998 |
| Source dataset | uspto-grants-1997_01 |
| ORD ID | ord-cab2cceda4484f56bccd489b4a522de9 |
| Source note | uspto-grants-1997_01 |