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HRID 6588作成日:2026年10月26日

3,4-dihydro-2H-pyran → 2-(4-Bromobutoxy)tetrahydro-2H-pyran

https://huagongshe.com/reaction/6588

反応式

関与物質

役割名称HCID仕込み量
反応物3,4-dihydro-2H-pyranHCID 8080—
反応物Potassium CarbonateHCID 11430—
反応物4-BromobutanolHCID 118388—
溶媒DichloromethaneHCID 6344—
溶媒Phosphorus oxychlorideHCID 24813—
生成物2-(4-Bromobutoxy)tetrahydro-2H-pyranHCID 559019—

反応手順

To a solution of commercially available 4-bromobutan-1-ol (16) (1 equi.) and 3,4-dihydropyran (17) (1.5 equi.) in dichloromethane (3 mL/mmole), phosphorus oxychloride (0.01 equi.) was added at room temperature. The reaction mixture was stirred at that temperature for 24 h. Then potassium carbonate (1 equi.) was added to the reaction mixture and the reaction mixture was stirred at room temperature for 1 h, quenched with water, extracted with dichloromethane, washed with brine, dried over MgSO4, and concentrated in vacuo. Purification by chromatography on silica gel (5% EtOAc (ethylacetate)/hexanes) afforded 2-(4-bromobutoxy) -tetrahydropyran (18), as a colorless oil (88%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07083832B2
出典データセットuspto-grants-2006_08
ORD IDord-9c10f800168b48649bfb59f8e3d09d94
出典メモuspto-grants-2006_08