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HRID 1726881作成日:2026年10月26日

Piperidine → 1-(4-Iodobenzoyl)piperidine

https://huagongshe.com/reaction/1726881

反応式

関与物質

役割名称HCID仕込み量
反応物PiperidineHCID 8082—
反応物4-Iodobenzoic acidHCID 12085—
反応物DiisopropylethylamineHCID 81531—
反応物O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
溶媒DichloromethaneHCID 6344—
生成物1-(4-Iodobenzoyl)piperidineHCID 5149204—

反応手順

To a suspension of 4.0 g of 4-iodobenzoic acid (16.13 mmol) in 40 ml of CH2Cl2 there are added 3.65 ml of diisopropylethylamine (20.97 mmol) and then, after 10 minutes, 5.18 g of TBTU (16.13 mmol). After stirring for 10 minutes more, 1.60 ml of piperidine (16.13 mmol) are added and the reaction mixture is stirred overnight at ambient temperature. The reaction mixture is washed 3 times with water and then once with saturated NaCl. After drying (MgSO4) and evaporation under reduced pressure, the residue is chromatographed on silica (CH2Cl2/acetone 9/1) to yield the title product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07494994B2
出典データセットuspto-grants-2009_02
ORD IDord-d608cb7ddaa847de967183dd61927261
出典メモuspto-grants-2009_02