HuagongsheHuagongshe Chemistry Print Report · For research reference only
N,N-Dimethylaniline → 2-Butyrylamino-4-methyl-3-nitropyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | Butyryl chloride | HCID 8855 | — |
| Reactant | 2-Amino-4-methyl-3-nitropyridine | HCID 243166 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Butyrylamino-4-methyl-3-nitropyridine | HCID 21464239 | — |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
A mixture of 2-amino-4-methyl-3-nitropyridine (5.0 g) and N,N-dimethylaniline (8.5 ml) was heated at 100° C. under nitrogen atmosphere. To the solution was added butyryl chloride (3.5 ml) and the mixture was stirred at 100° C. for 5 hours. After being cooled to room temperature, ethyl acetate was added to the reaction mixture. The organic layer was separated and washed successively with water and brine. The solution was dried over magnesium sulfate and the solvent was evaporated in vacuo. The residue was washed with n-hexane to give 2-butyrylamino-4-methyl-3-nitropyridine (7.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05215994 |
| Source dataset | uspto-grants-1993_06 |
| ORD ID | ord-c713399dc6584bccab1178e0da344317 |
| Source note | uspto-grants-1993_06 |