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HRID 2111988作成日:2026年10月25日

3-Fluoro-4-hydroxybenzeneacetic acid → N-Benzyl-2-(3-fluoro-4-hydroxyphenyl)-N-hexylacetamide

https://huagongshe.com/reaction/2111988

反応式

関与物質

役割名称HCID仕込み量
反応物3-Fluoro-4-hydroxybenzeneacetic acidHCID 68014—
反応物DiisopropylethylamineHCID 81531—
反応物Benzenemethanamine, N-hexyl-HCID 485395—
反応物O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
溶媒DimethylformamideHCID 6228—
生成物N-Benzyl-2-(3-fluoro-4-hydroxyphenyl)-N-hexylacetamideHCID 6887125777.2%

反応手順

3-Fluoro-4-hydroxyphenylacetic acid (170 mg, 0.999 mmol) dissolved in DMF (3 ml) was cooled in an ice-bath N-Hexylbenzylamine (201 mg, 1.049 mmol) was added and then TBTU (337 mg, 1.049 mmol) followed by DIPEA (407 mg, 3.147 mmol). The mixture was stirred at room temperature overnight and evaporated. Sodium hydrogencarbonate aqueous solution (sat.) was added into the residue. The mixture was then extracted with ethyl acetate (×2). The extracts were combined and washed with water and brine and dried (magnesium sulphate) and evaporated. Chromatography of the residue on a column (ISOLUTE® SI, 5 g/15 ml) using DCM and then MeOH/DCM (1:99) as eluant gave 265 mg the desired product, yield 77%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07521461B2
出典データセットuspto-grants-2009_04
ORD IDord-cc98671f87b84a8e8507afecc439120f
出典メモuspto-grants-2009_04