化工社化工社 化学情報印刷レポート · 研究参考用
Sodium hydride → (2S,4R)-N-Boc-4-(4-Bromobenzyloxy)-2-methyl-proline
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | 4-Bromobenzyl bromide | HCID 68527 | — |
| 反応物 | 1-(tert-Butyl) 2-methyl (2S,4R)-4-hydroxy-2-methylpyrrolidine-1,2-dicarboxylate | HCID 10635010 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | (2S,4R)-N-Boc-4-(4-Bromobenzyloxy)-2-methyl-proline | HCID 21301005 | 28.4% |
反応手順
To a suspension of sodium hydride (60% in oil) (0.12 g) (1.5 eq.) in 5 mL of dry THF was added (2S,4R)-N-Boc-4-hydroxy-2-methyl-proline methyl ester (0.55 g) in 5 mL of dry THF. The reaction mixture was stirred for 45 min., and a solution of 4-bromobenzyl bromide (0.75 g) (1.5 eq.) in 5 mL of dry THF was added. The reaction mixture was refluxed for 3 h. After cooling to RT, the reaction mixture was diluted with water and extracted with EtOAc. The aqueous layer was acidified and extracted with DCM. The combined organic extracts were washed with water, dried over MgSO4 and evaporated under reduced pressure to afford (2S,4R)-N-Boc-4-(4-bromo-benzyloxy)-2-methyl-proline (0.25 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06710064B2 |
| 出典データセット | uspto-grants-2004_03 |
| ORD ID | ord-2d29d28f58b24fcfa52d6529402a7cce |
| 出典メモ | uspto-grants-2004_03 |