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4-tert-Butylbenzyl alcohol → 4-(4-t-Butylbenzyloxy)-5-methoxypyrimidine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-tert-Butylbenzyl alcohol | HCID 13416 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | 4-Chloro-5-methoxypyrimidine | HCID 11008039 | — |
| 溶媒 | Dimethylacetamide | HCID 31374 | — |
| 生成物 | 4-(4-t-Butylbenzyloxy)-5-methoxypyrimidine | HCID 76853235 | 77% |
反応手順
To a solution of 4-chloro-5-methoxypyrimidine (1.5 g, 10.3 mmol) described in Journal of the Chemical Society (1960), 4590, and 4-t-butylbenzylalcohol (2.55 g, 15.6 mmol) in dimethylacetamide (10 mL) was added sodium hydride (0.625 g, 15.6 mmol) at 0° C., and the mixture was stirred at room temperature for 3 hrs. The reaction mixture was poured into ice water, and 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-t-butylbenzyloxy)-5-methoxypyrimidine (2.16 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08895574B2 |
| 出典データセット | uspto-grants-2014_11 |
| ORD ID | ord-93733c3d90984d0eb0ecac29f21d3b54 |
| 出典メモ | uspto-grants-2014_11 |