HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetaldehyde → 2,3,6-Trimethylpyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Propanal | HCID 527 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 2,6-Lutidine | HCID 7937 | — |
| Reactant | 3-Methylpyridine | HCID 7970 | — |
| Reactant | 3,5-Dimethylpyridine | HCID 11565 | — |
| Reactant | Pyridine, 2,6-diethyl-3-methyl- | HCID 12317250 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Solvent | Ethyl ketone | HCID 7288 | — |
| Product | 2,3,6-Trimethylpyridine | HCID 15100 | — |
Reaction Steps
Such pyridine bases as pyridine, picoline, lutidine, collidine, etc. can be produced in the present invention. For example, when formaldehyde and acetaldehyde are used together with ammonia, pyridine and 3-picoline are obtained. When formaldehyde and propionaldehyde are used together with ammonia, 3,5-lutidine and a small amount of 3-picoline are obtained. When formaldehyde, acetaldehyde and propionaldehyde are used together with ammonia, pyridine, 3-picoline and 3,5-lutidine are obtained. Further, when formaldehyde and acetone are used together with ammonia, 2,6-lutidine is principally obtained. When diethylketone or methylethylketone is used together with ammonia, 2,6-diethyl-3-methylpyridine or 2,3,6-trimethylpyridine is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03946020 |
| Source dataset | uspto-grants-1976_03 |
| ORD ID | ord-a7edcba52f3744a184e486304a755982 |
| Source note | uspto-grants-1976_03 |