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HRID 81164作成日:2026年10月27日

Benzylamine → trans-4-(Benzylamino)tetrahydrofuran-3-ol

https://huagongshe.com/reaction/81164

反応式

関与物質

役割名称HCID仕込み量
反応物BenzylamineHCID 7504—
反応物Ethyl AcetateHCID 8857—
反応物Ammonium ChlorideHCID 25517—
反応物3,6-Dioxabicyclo[3.1.0]hexaneHCID 67511—
触媒HCID 178460666HCID 178460666—
生成物trans-4-(Benzylamino)tetrahydrofuran-3-olHCID 86724519—

反応手順

Ti(OiPr)4 (1.0 mL, 3.48 mmol) was added to a solution of 3,6-dioxabicyclo[3.1.0]hexane (1.5 g, 17.4 mmol) in benzylamine (2.0 mL). The mixture was irradiated in a microwave reactor at 130° C. for 2 hours. It was cooled to room temperature, and 50 mL of saturated aqueous NH4Cl solution and 20 mL of EtOAc were added to the reaction. The mixture was stirred for 10 minutes. The resulting gummy precipitate was filtered over a celite bed, and the filtrate was extracted using EtOAc (100 mL). The organic layer was separated, washed with brine, dried over anhydrous Na2SO4, filtered, and concentrated in vacuo. The residue was purified by reverse phase chromatography on a C-18 column (0-100% CH3CN/water) to afford trans-4-(benzylamino) tetrahydrofuran-3-ol. MS APCl calc'd for C11H15NO2 [M+H]+ 194. found 194.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846657B2
出典データセットuspto-grants-2014_09
ORD IDord-5b84ec78922c42d49a739441b7ccf017
出典メモuspto-grants-2014_09