戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 49979作成日:2026年10月25日

Sodium hydride → (2S,4R)-N-Boc-4-(4-Bromobenzyloxy)-2-methyl-proline

https://huagongshe.com/reaction/49979

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物4-Bromobenzyl bromideHCID 68527—
反応物1-(tert-Butyl) 2-methyl (2S,4R)-4-hydroxy-2-methylpyrrolidine-1,2-dicarboxylateHCID 10635010—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物(2S,4R)-N-Boc-4-(4-Bromobenzyloxy)-2-methyl-prolineHCID 2130100528.4%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US06710064B2
出典データセットuspto-grants-2004_03
ORD IDord-2d29d28f58b24fcfa52d6529402a7cce
出典メモuspto-grants-2004_03