HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formamidine acetate → 5-(p-Methoxyphenoxy)pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formamidine acetate | HCID 160693 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 2-(p-Methoxyphenoxy)-3-(dimethylamino)acrolein | HCID 54498024 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-(p-Methoxyphenoxy)pyrimidine | HCID 20292632 | 64.8% |
Reaction Steps
Sodium metal (4.1 g) was dissolved in absolute ethanol (90 ml) and formamidine acetate (18.4 g) and 2-(p-methoxyphenoxy)-3-(dimethylamino)acrolein (13.0 g) were added to the ethanolic solution of sodium ethoxide. The mixture was heated under reflux, with stirring, for 40 hr and then the solvent was removed, by distillation under reduced pressure. The residue was treated with water (200 ml) and chloroform (200 ml), the chloroform layer was separated and the chloroform removed by distillation under reduced pressure. The residue was purified by column chromatography over silica gel using chloroform as eluent to give 5-(p-methoxyphenoxy)pyrimidine as an oil (7.7 g) which was characterised by p.m.r. spectroscopy.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04248618 |
| Source dataset | uspto-grants-1981_02 |
| ORD ID | ord-7c9c18fa35224396956b3055bc705172 |
| Source note | uspto-grants-1981_02 |