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HRID 1830725作成日:2026年10月27日

Tetrahydrofuran → (1-Benzyl-4-piperidyl)methanamine

https://huagongshe.com/reaction/1830725

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物N-benzylpiperidine-4-carboxamideHCID 3868064—
反応物Aluminium lithium hydrideHCID 21226445—
生成物(1-Benzyl-4-piperidyl)methanamineHCID 1514444—

反応手順

To a solution of N-benzylisonipecotamide (7.34g, 34 mmol) in 60 mL of anhydrous THF, was added, LiAlH4 (1.9 g, 51 mmol) and the mixture was stirred at room temperature for 10 minutes followed by heating to reflux for 3 h. The reaction was quenched by addition of 100 mL sat'd. sodium potassium tartrate, and was extracted with EtOAc (3×50 mL). The combined extracts were washed with 20 mL water and 20 mL brine then dried over MgSO4, filtered and concentrated to give the desired product. 1H-NMR (400 MHz, CDCl3) δ7.13 (m, 5H), 3.42 (s, 2H), 2H), 2.91 (m, 2H), 2.59 (m, 2H), 1.97 (m, 2H), 1.62 (m, 2H), 2.21 (m, 5H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07067506B2
出典データセットuspto-grants-2006_06
ORD IDord-5853d05e12d34035b74547b4333db766
出典メモuspto-grants-2006_06