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HRID 2080254作成日:2026年10月27日

5-Benzylfuran-2-carbaldehyde → 5-(Phenylmethyl)-2-furanmethanamine

https://huagongshe.com/reaction/2080254

反応式

関与物質

役割名称HCID仕込み量
反応物5-Benzylfuran-2-carbaldehydeHCID 12418537—
反応物Ammonia methanolHCID 21705897—
触媒NickelHCID 935—
生成物5-(Phenylmethyl)-2-furanmethanamineHCID 2313062065.8%

反応手順

7N Ammonia/methanol(40 mL) and Raney nickel(3 g) were added to 5-benzyl-furan-2-carbaldehyde described in Preparation Example 39 (2.5 g, 13 mmol), and the solution was stirred for 22 hours under hydrogen atmosphere at room temperature. After removing the catalyst by filtering through Celite pad, the solvent was evaporated in vacuo and C-(5-benzyl-furan-2-yl)methylamine (1.6 g, 8.6 mmol, 65.8%) was obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07932272B2
出典データセットuspto-grants-2011_04
ORD IDord-fa9049e0f9524da9bf4ee48ab4ee6885
出典メモuspto-grants-2011_04