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HRID 2336作成日:2026年10月24日

Borane;tetrahydrofuran → Methyl 3-(piperidin-1-yl)benzoate

https://huagongshe.com/ja/reaction/2336

反応式

関与物質

役割名称HCID仕込み量
反応物Borane;tetrahydrofuranHCID 2723981—
反応物Methyl 3-(2-oxopiperidin-1-yl)benzoateHCID 10681135—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 3-(piperidin-1-yl)benzoateHCID 714841390%

反応手順

The compound of Example 37 (640 mg, 2.75 mmol) was dissolved in dry THF (30 ml) and borane-tetrahydrofuran complex (5 ml, 1M solution in THF) was added. The mixture was stirred under nitrogen under reflux for 1 h, then cooled and evaporated. The residue was taken up in MeOH/acetic acid (6/1, v/v, 70 ml) and heated under reflux for 3 h, then evaporated and chromatographed (eluant 10% EtOAc in hexanes) to provide a colourless oil (540 mg, 90%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05728829
出典データセットuspto-grants-1998_03
ORD IDord-b2a2fb45af4f44099c49615f8d09865c
出典メモuspto-grants-1998_03