HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → 1-(2,4,6-Trimethyl-3-pyridinyl)-1,3-butanedione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 3-Acetyl-2,4,6-trimethylpyridine | HCID 268124 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 1-(2,4,6-Trimethyl-3-pyridinyl)-1,3-butanedione | HCID 53771125 | 86% |
Reaction Steps
A mixture of 172.0 g of 3-acetyl-collidine, 4.5 l of anhydrous toluene, 195 g of ethyl acetate and 282.5 g of potassium tert.-butylate is heated at 100° for 4 hours under nitrogen. The reaction mixture is cooled and poured into 1/2 l of ice water and 140 ml of acetic acid, and the phases are separated and worked up in the customary manner to give 186.1 g of 2,4,6-trimethyl-nicotinoyl-acetone ##SPC8##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03969363 |
| Source dataset | uspto-grants-1976_07 |
| ORD ID | ord-6c881ff38ad5451ca864df52c054bf45 |
| Source note | uspto-grants-1976_07 |