戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 38299作成日:2026年10月26日

Benzyl Bromide → Tert-butyl 4-benzyl-3-oxopiperazine-1-carboxylate

https://huagongshe.com/reaction/38299

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl BromideHCID 7498—
反応物Sodium hydrideHCID 24758—
反応物Tert-butyl 3-oxopiperazine-1-carboxylateHCID 3157178—
溶媒DimethylformamideHCID 6228—
生成物Tert-butyl 4-benzyl-3-oxopiperazine-1-carboxylateHCID 10891590—

反応手順

Sodium hydride (88 mg, 60% wt.) was added portionwise to a solution of 4-BOC-piperazinone (400 mg) in DMF (10 ml). The reaction mixture was stirred for 1 h, and then benzyl bromide (262 μl) was added dropwise and the mixture stirred at room temp for 16 h. The reaction was quenched with methanol and diluted with water, and then extracted with EtOAC. The organic extracts were concentrated in vacuo and the residue was purified by chromatography (silica, 20% ether/hexane as eluent) to give the sub-title compound (429 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524715B2
出典データセットuspto-grants-2013_09
ORD IDord-986826fa224b44c498e4e63b28714e72
出典メモuspto-grants-2013_09