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HRID 1167033作成日:2026年10月24日

Cyclohexanone → 1-Cyclohexylpyrrolidine

https://huagongshe.com/ja/reaction/1167033

反応式

関与物質

役割名称HCID仕込み量
反応物CyclohexanoneHCID 7967—
反応物Sulfuric acid magnesium salt (1:1)HCID 24083—
反応物PyrrolidineHCID 31268—
溶媒HexaneHCID 8058—
生成物1-CyclohexylpyrrolidineHCID 139064—

反応手順

The structure-directing agent (SDA) is synthesized using the reaction sequence described in the scheme below. A three neck 3 000-ml flask is charged with 100 gm (1.4 mole) of pyrrolidine, 50 gm of cyclohexanone (0.51 mole) and 1000 ml anhydrous hexane. To the resulting solution, 122 gm (1.022 mole) of anhydrous magnesium sulfate is added and the mixture is mechanically stirred and heated at reflux (the reaction is monitored by NMR analysis) for 96 hrs. The reaction mixture is filtered through a fritted glass funnel. The filtrate is concentrated under reduced pressure on a rotary evaporator to give 75 gm of a clear (yellow-tinted) oily substance. 1H-NMR and 13C-NMR spectra are acceptable for the desired product 1-(1-pyrrolidino)cyclohexene. Saturation of 1-(1-pyrrolidino)cyclohexene, to give N-cyclohexylpyrrolidine, is accomplished in quantitative yield by hydrogenation in ethanol at a 55 psi pressure of hydrogen gas in the presence of 10% Pd on activated carbon.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06616830B2
出典データセットuspto-grants-2003_09
ORD IDord-daf53d9553b44280b7361cf574f31ae2
出典メモuspto-grants-2003_09