HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phosphorus oxychloride → 2-tert-Butyl-4-chloro-6-cyclopropyl-pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 178441865 | HCID 178441865 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-tert-Butyl-4-chloro-6-cyclopropyl-pyrimidine | HCID 63355304 | 104.9% |
Reaction Steps
14.8 g 2-tert-butyl-4-hydroxy-6-cyclopropyl-pyrimidine (76.9 mmol) were dissolved in 100 ml of toluene and 3 ml of dimethylformamide. 23.6 ml of POCl3 (153.7 mmol) were added dropwise at 10° C. After stirring overnight at room temperature most of the toluene was evaporated. The mixture was cooled with ice and 20 ml of water were added cautiously. Subsequently, an additional 200 ml of water were added and the aqueous phase was extracted four times with dichloromethane. The combined organic phases were dried over magnesium sulfate, filtered, and then concentrated to dryness to yield 17 g of a yellowish oil (quant.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08202868B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-8f760cff3ce9466ea5589371ac324223 |
| Source note | uspto-grants-2012_06 |