HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → 2-{6-Chloro-5-(4-methylphenyl)pyrimidin-4-yloxy}ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4,6-Dichloro-5-(4-methylphenyl)pyrimidine | HCID 21979554 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-{6-Chloro-5-(4-methylphenyl)pyrimidin-4-yloxy}ethanol | HCID 11118967 | — |
Reaction Steps
To a mixture of tetrahydrofuran (400 ml) and ethylene glycol (60 ml) is added with stirring sodium hydride (60% dispersion, 3.38 g) under ice-cooling, and thereto is added 4,6-dichloro-5-(4-methylphenyl)pyrimidine (20.0 g). The mixture is stirred under ice-cooling for 30 minutes, and then stirred at room temperature for two hours. The mixture is weakly acidified with acetic acid, and concentrated under reduced pressure. The residue is dissolved in ethyl acetate, and washed, dried, and concentrated to dryness under reduced pressure. The residue is crystallized from hexane to give 2-{6-chloro-5-(4-methylphenyl)pyrimidin-4-yloxy}ethanol (21.85 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05739333 |
| Source dataset | uspto-grants-1998_04 |
| ORD ID | ord-443b6a410d644885b063dcd42d3ef063 |
| Source note | uspto-grants-1998_04 |