Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | HCID 13799476 | HCID 13799476 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 20213009 | HCID 20213009 | — |
Reaction Steps
A suspension of 5.0 g of 6-chloro-2-hydrazinopyridine-4-carbonitrile in 50 ml of pyridine was cooled to 0° C. in an ice bath and 3.1 g of acetyl chloride was added dropwise over a 10 minute period. The mixture became homogeneous after the addition and it was allowed to warm to ambient temperature. After 2 hours, the reaction mixture was poured into 180 ml of water and the precipitate which formed was separated by filtration and dried to give N-acetyl-N'-(6-chloro-4-cyano-2-pyridyl)hydrazine which was purified by recrystallization from ethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04650872 |
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| Source dataset | uspto-grants-1987_03 |
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| ORD ID | ord-da48261b9fe440c0b6af20f085874e05 |
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| Source note | uspto-grants-1987_03 |
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