Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Reactant | HCID 178429399 | HCID 178429399 | — |
| Catalyst | Zinc Acetate | HCID 11192 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178433163 | HCID 178433163 | — |
Reaction Steps
382.5 Parts of 2-dimethylamino-4-hydroxy-6-methylpyrimidine, 50 parts of zinc acetate and 35 parts of a 50% aqueous paste of a 3% palladium on carbon catalyst are stirred in 2500 parts of acetic acid and 1000 parts of water in a closed container. Hydrogen is then passed into the reaction vessel to a pressure of 3 bar and the temperature is raised to 100° C. 285 parts of 36% formaldehyde diluted with 500 parts of water are added over 6 hours, maintaining a hydrogen pressure of 3 bar and temperature of 98°- 100° C., followed by the addition of 1075 parts of water. The reaction mixture is stirred under these conditions for a further 17 hours, and then cooled and the palladium on carbon catalyst is removed by filtration. The filtrates are distilled under reduced pressure to remove water and acetic acid and to the residue 2500 parts of water and 150 parts of 32% sodium hydroxide solution are added. The suspension is heated to 60° C. and filtered, the filter cake washed with 22 parts of 32% sodium hydroxide solution diluted with 1000 parts of water. The combined filtrates and washes are adjusted to pH 6 with 100 parts of 35% hydrochloric acid and extracted with chloroform. The chloroform is removed by distillation to yield 283 parts of 2-dimethylamino-4,5-dimethyl-6-hydroxypyrimidine, analysing at 95% strength.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US03947440 |
|---|
| Source dataset | uspto-grants-1976_03 |
|---|
| ORD ID | ord-471a3204731a4da3a6a3397425a834ab |
|---|
| Source note | uspto-grants-1976_03 |
|---|