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HRID 1645542作成日:2026年10月27日

Dimethylformamide → 5-Benzyloxy-2,2-dimethyl-1,3-dioxane

https://huagongshe.com/reaction/1645542

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Benzyl BromideHCID 7498—
反応物Sodium hydrideHCID 24758—
反応物2,2-Dimethyl-1,3-dioxan-5-olHCID 11029884—
触媒Tetrabutylammonium IodideHCID 67553—
溶媒WaterHCID 962—
生成物5-Benzyloxy-2,2-dimethyl-1,3-dioxaneHCID 2036488954.5%

反応手順

To a N,N-dimethylformamide (200 ml) solution of the 2,2-dimethyl-1,3-dioxan-5-ol (7.1 g, 0.054 mol) obtained in the step (9a), sodium hydride, in oil (2.81 g, 0.064 mol as the content was regarded as 55%) was added at 0° C. and stirred. After benzyl bromide (12.9 ml, 0.108 mol) and tetrabutylammonium iodide (220 mg, 0.001 mol) were added at the same temperature to the mixture, the mixture was stirred at room temperature for 1.5 hours. Water was added to the reaction mixture, which was then extracted with ethyl acetate three times. Organic layers were combined, washed five times with water and once with a saturated saline solution, dried over anhydrous sodium sulfate, and filtered. After NH silica gel was added, the resultant mixture was concentrated and purified by silica gel column chromatography (elution solvent: heptane, heptane/ethyl acetate=9/1, 4/1, ethyl acetate) to obtain the title compound (6.5 g, 54.5%) as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08124780B2
出典データセットuspto-grants-2012_02
ORD IDord-3ed6ca2a0d234cbb978cc9a7de249aba
出典メモuspto-grants-2012_02