HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → HCID 86698875, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-(Trifluoromethyl)benzenemethanol | HCID 67684 | — |
| Reactant | HCID 21557075 | HCID 21557075 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 86698875 | HCID 86698875 | 91.2% |
Reaction Steps
To a solution of 4-chloro-5-phenoxypyrimidine (0.4 g, 1.9 mmol) described in JP-A-49-92080 and 4-trifluoromethylbenzylalcohol (0.36 g, 2.0 mmol) in dimethylacetamide (7 m) was added sodium hydride (0.093 g, 2.3 mmol) at 0° C., and the mixture was stirred at room temperature for 3 hrs. The reaction mixture was poured into ice water, and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give 4-(4-trifluoromethylbenzyloxy)-5-phenoxypyrimidine (0.60 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08895574B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-51e9ec9cda2a4995aa70de870b2f18e0 |
| Source note | uspto-grants-2014_11 |