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HRID 2190256作成日:2026年10月27日

tert-Butyl piperazine-1-carboxylate → tert-Butyl 4-((3-bromofuran-2-yl)methyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/2190256

反応式

関与物質

役割名称HCID仕込み量
反応物tert-Butyl piperazine-1-carboxylateHCID 143452—
反応物3-Bromo-2-furaldehydeHCID 3367271—
反応物Sodium triacetoxyborohydrideHCID 5049666—
溶媒DichloromethaneHCID 6344—
溶媒Ethyl AcetateHCID 8857—
生成物tert-Butyl 4-((3-bromofuran-2-yl)methyl)piperazine-1-carboxylateHCID 7107912892.5%

反応手順

To a solution of 3-bromofuran-2-carbaldehyde (500 mg, 2.85 mmol) and tert-butyl piperazine-1-carboxylate (1.1 g, 5.71 mmol) in CH2Cl2 (10 mL) was added sodium triacetoxyborohydride (1.2 g, 5.71 mmol). The mixture was stirred at room temperature for 12 hours. The reaction mixture was diluted with EtOAc (100 mL). The organic phase was washed with aqueous NaHCO3 and brine then dried (MgSO4), filtered and concentrated to dryness. The residue was purified by column chromatography (silica, 0-10% MeOH in CH2Cl2) to afford the sub-title compound (910 mg, 92%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08324264B1
出典データセットuspto-grants-2012_12
ORD IDord-21fe05743de049d4a49b049ec970359d
出典メモuspto-grants-2012_12