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tert-Butylacrylamide → HCID 14297377、化合物
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | tert-Butylacrylamide | HCID 7877 | — |
| 反応物 | Dibenzylhydroxylamine | HCID 69297 | — |
| 反応物 | Potassium tert-butoxide | HCID 23665647 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | HCID 14297377 | HCID 14297377 | — |
反応手順
A solution of 21.33 g of dibenzylhydroxylamine in 100 ml of dry tetrahydrofuran is admixed with 1.12 g of potassium-tert-butoxide followed by 12.70 g of N-tert-butylacrylamide. The solution is heated under reflux for 24 hours under N2. The crude reaction mixture is concentrated under reduced pressure and the residue is partitioned between water and methylene chloride. The organic layer is washed with water, brine dried (MgSO4) and evaporated under reduced pressure. Purification by liquid chromatography affords the title compound as an oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04760179 |
| 出典データセット | uspto-grants-1988_07 |
| ORD ID | ord-ae0ad8f5f7034c5786f95eee030825cc |
| 出典メモ | uspto-grants-1988_07 |