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HRID 1641854作成日:2026年10月26日

p-Fluoronitrobenzene → Methyl 1-(4-nitrophenyl)piperidine-4-carboxylate

https://huagongshe.com/reaction/1641854

反応式

関与物質

役割名称HCID仕込み量
反応物p-FluoronitrobenzeneHCID 9590—
反応物DiisopropylethylamineHCID 81531—
反応物Methyl isonipecotateHCID 424914—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 1-(4-nitrophenyl)piperidine-4-carboxylateHCID 34500237.4%

反応条件

温度150 °C

反応手順

To a solution of 4-fluoronitrobenzene (0.70 g, 4.96 mmol) in THF (8 mL) was added piperadine-4-carboxylic acid methyl ester (0.71 g, 4.96 mmol) and diisopropylethylamine (0.66 g, 5.11 mmol). The mixture was heated in a microwave oven at 150° C. for 1.5 hr. The resulting mixture was extracted with ethyl acetate and hydrochloric acid (0.2 N). The organic layer was washed with brine and concentrated sodium bicarbonate solution. After the evaporation of solvents, the residue was purified through a Biotage flash column chromatography using ethyl acetate and hexanes (1:1 ratio) to give a yellow solid as 1-(4-nitrophenyl)-piperidine-4-carboxylic acid methyl ester (490 mg). 1H-NMR is consistent with the structure.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08115011B2
出典データセットuspto-grants-2012_02
ORD IDord-e70ec3731a904dd5af0c318acc04c0d5
出典メモuspto-grants-2012_02