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HRID 33467作成日:2026年10月23日

5-Nitrofurfural → 5-(Nitro-furan-2-ylmethyl)-(2-piperidin-1-yl-phenyl)-amine

https://huagongshe.com/ja/reaction/33467

反応式

関与物質

役割名称HCID仕込み量
反応物5-NitrofurfuralHCID 12774—
反応物2-(Piperidin-1-yl)anilineHCID 458795—
反応物Sodium triacetoxyborohydrideHCID 5049666—
溶媒DichloromethaneHCID 6344—
生成物5-(Nitro-furan-2-ylmethyl)-(2-piperidin-1-yl-phenyl)-amineHCID 86595722—

反応手順

A solution of 2-piperidinoaniline (1 mmol), 5-nitro-furan-2-carbaldehyde (1.1 mmol) and sodium triacetoxyborohydride (“NaBH(OAc)3”) (2 mmol) in anhydrous DCM (10 mL) was stirred 16 h at room temperature. The mixture was then washed successively with water, dilute aqueous sodium hydroxide (“NaOH”), water and brine before being dried over MgSO4, filtered and concentrated under reduced pressure. Purification of the residual oil by flash silica gel chromatography yielded the product. MS: 301 (M+1). LC/MS purity: 100%. 1H NMR (CDCl3, 300 MHz): δ 7.25 (d, 1H), 7.15-6.95 (m, 2H), 6.75 (t, 1H), 6.55 (d, 1H), 5.4 (bs, 1H), 4.45 (s, 2H), 2.8 (bm, 4H), 1.8-1.5 (bm, 6H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07429603B2
出典データセットuspto-grants-2008_09
ORD IDord-f1581ed5899248c99cc9d8b5f38f94e0
出典メモuspto-grants-2008_09