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HRID 2210024作成日:2026年10月27日

Piperidine → 2-Nitro-5-(piperidin-1-yl)benzoic acid

https://huagongshe.com/reaction/2210024

反応式

関与物質

役割名称HCID仕込み量
反応物PiperidineHCID 8082—
反応物5-Chloro-2-nitrobenzoic acidHCID 17286—
溶媒DimethylacetamideHCID 31374—
生成物2-Nitro-5-(piperidin-1-yl)benzoic acidHCID 14459331—

反応条件

温度120 °C

反応手順

A mixture of 5-chloro-2-nitrobenzoic acid (13.7 g), piperidine (27 ml) and DMA (100 ml) was stirred and heated to 120° C. for 18 hours. The mixture was evaporated. The residue was dissolved in water and the solution was basified to pH10 by the addition of 2N aqueous sodium hydroxide solution. The solution was extracted with ethyl acetate. The aqueous layer was acidified to pH2 by the addition of concentrated hydrochloric acid and extracted with ethyl acetate. The organic layer was dried (MgSO4) and evaporated to give 2-nitro-5-piperidinobenzoic acid (16.25 g), m.p.130°-140° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05457105
出典データセットuspto-grants-1995_10
ORD IDord-4680114c0a014396afdb5c5fc66f4162
出典メモuspto-grants-1995_10